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Spine

Spine implants for cervical, lumbar, and a variety of procedures.

Spine implants most often used in spine surgeries and available in many different sizes to fit various applications. Our tissue grafts and spine implants are clincally proven in more applications than any other allograft spine implant provider. As a result, we are the world's most trusted provider of transplant solutions, from new innovations in tissue grafts and spine implants, to regenerative medicine and cellular therapies. Nearly 5 million tissue grafts have been distributed with no disease transmission since the introduction of Allowash XG®. Click the below links to browse our wide portfolio of spine implants and tissue grafts for void/defects.

To download or print our full line of allograft bio-implants click here.
 

Spine

  1. Cervical
    1. Fibular Wedges
    2. VertiGraft Fibular Spacer
    3. VG1® Cervical
    4. VG2® Cervical
    5. Cloward Dowel
    6. Tricortical Cancellous Wedge - Parallel
    7. Unicortical Cancellous Spacer - Parallel
    8. VG1® Laminoplasty Spacer
    9. Iliac Crest Wedge
    10. ACIS VG2™
  2. Biologics
    1. Cortical/Cancellous Chips
    2. I/C Graft Chamber®
    3. Demineralized Cancellous Chips
    4. Demineralized Cortical Powder
    5. Fascia Lata
    6. Pericardium
    7. Optium® DBM Putty
    8. Optium DBM® Gel
    9. Demineralized Cortical/Cancellous
    10. Demineralized Fibers
    11. Cancellous Chips
    12. PliaFX® Strip
  3. Lumbar
    1. VG1® ALIF
    2. VertiGraft® Humeral Spacer
    3. VG2® PLIF
    4. VG2® RAMP
    5. VG2® TLIF
  4. Corpectomy
    1. VertiGraft Fibular Shafts
    2. Humeral - Shafts
    3. Tibial - Shafts
    4. Femoral - Shafts
    5. Humeral - Shafts
Description
MatriGRAFT® Fibular Wedge, parallel cross-section processed from the fibula, radius or ulna
  • Pre-sized for convenience
  • Allows physician to supplement with additional graft material
  • Allows for structural support
  • Allows physician to select appropriate graft for clinical procedure
  • Provides an osteoconductive matrix for incorporation

Specification Sheets: 

Clinical Application
  • Anterior Cervical Fusion
  • Trauma

Fibular Segment, VertiGraft® Fibula/Radius/Ulna Wedge

FrozenDescriptionSize
FFIBW8

Fibula/Radius/Ulna Wedge

H = 18 mm
Freeze-DriedDescriptionSize
FIBW0.6

Fibula/Radius/Ulna Wedge

H = 6 mm
FIBW0.8

Fibula/Radius/Ulna Wedge

H = 8 mm
FIBW1

Fibula/Radius/Ulna Wedge

H = 10 mm
FIBW2

Fibula/Radius/Ulna Wedge

H = 12 mm
FIBW4

Fibula/Radius/Ulna Wedge

H = 14 mm
FIBW6

Fibula/Radius/Ulna Wedge

H = 16 mm
FIBW8

Fibula/Radius/Ulna Wedge

H = 18 mm
68-60-128.pdf
Description

Solid one piece cortical spacer designed to provide biomechanical strength for spinal fusion inter-body and discectomy procedures

  • Strength: Cortical Construction
  • Stability: Textured surface area to reduce migration
  • Variety: Multiple footprints in both parallel and lordotic configurations to better match patient anatomy
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1
  • Convenience: Freeze-dried for room temperature storage
Clinical Application
  • Spinal fusion inter-body and discectomy procedures
Freeze-DriedDescriptionSize
VFIBCS15

Fibular Spacer Parallel

Anterior Height = 5 mm
VFIBCS16

Fibular Spacer Parallel

Anterior Height = 6 mm
VFIBCS17

Fibular Spacer Parallel

Anterior Height = 7 mm
VFIBCS18

Fibular Spacer Parallel

Anterior Height = 8 mm
VFIBCS19

Fibular Spacer Parallel

Anterior Height = 9 mm
VFIBCS110

Fibular Spacer Parallel

Anterior Height = 10 mm
VFIBCS112

Fibular Spacer Parallel

Anterior Height = 12 mm
VFIBCS114

Fibular Spacer Parallel

Anterior Height = 14 mm
VFIBW5

Fibular Spacer Lordotic

Anterior Height = 8 mm
VFIBW7

Fibular Spacer Lordotic

Anterior Height = 10 mm
VFIBW9

Fibular Spacer Lordotic

Anterior Height = 12 mm
VFIBW11

Fibular Spacer Lordotic

Anterior Height = 11 mm
68-60-051-01.pdf
Description

Solid, one piece cortical implant designed to provide biomechanical strength for ACDF procedures

  • Solid, one piece cortical construction designed to provide biomechanical strength
  • Central void allows for physician preferred osteoinductive filler
  • Chamfered posterior surface and bulleted nose for ease of insertion
  • Stability: Textured surface designed to reduce migration
  • Variety: Multiple footprints in both parallel and lordotic configurations to better match patient anatomy
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1
  • Fully Hydrated, Ambient Storage Available: This implant features Preservon, a proprietary, glycerol-based preservation technology that allows allograft bio-implants to be stored in a fully hydrated state at ambient temperature. Preservon® eliminates lengthy rehydrating times, and does not require freezer storage2
  • Uniform dimensions

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
  2. Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data on file at LifeNet Health, Virginia Beach, VA.
Clinical Application
  • Anterior Cervical Discectomy and Fusion
  • VG2 Cervical
  • VertiGraft Fibular Spacer

 

PreservonDescriptionSize
VG1C-T46P

VG1® Cervical - 7° Lordosis

Anterior Height = 6 mm
VG1C-T57P

VG1® Cervical - 7° Lordosis

Anterior Height = 7 mm
VG1C-T68P

VG1® Cervical - 7° Lordosis

Anterior Height = 8 mm
VG1C-T79P

VG1® Cervical - 7° Lordosis

Anterior Height = 9 mm
VG1C-T810P

VG1® Cervical - 7° Lordosis

Anterior Height = 10 mm
VG1 CPAR6P

VG1 Cervical - Parallel

Anterior Height = 6 mm
VG1 CPAR7P

VG1 Cervical - Parallel

Anterior Height = 7mm
VG1 CPAR8P

VG1 Cervical - Parallel

Anterior Height = 8 mm
VG1 CPAR9P

VG1 Cervical - Parallel

Anterior Height = 9 mm
VG1 CPAR10P

VG1 Cervical - Parallel

Anterior Height = 10 mm
68-60-050-01.pdf
Description

Bio-implant designed with two cortical endplates supporting a cancellous center for ACDF procedures

  • Proven Clinical Performance: A prospective study found 100% fusion rates after 12 months in 74 ACDF patients1
  • Osteoconductive: Large cancellous matrix facilitates early bone growth
  • Stability: Textured surface designed to reduce migration
  • Variety: Multiple footprints in both parallel and lordotic configurations to better match patient anatomy
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties2
  • Ambient Storage Available: This implant features Preservon®; a proprietary, glycerol-based preservation technology that allows allograft bio-implants to be stored in a fully-hydrated state at ambient temperature. Preservon eliminates lengthy thawing and rehydrating times, and does not require freezer storage, or compromise biomechanical strength3
  • Uniform dimensions

 

  1. Abla, Adnan, et al. (2005) Allograft Composite Cortical and Cancellous Bone Graft for Anterior Cervical Fusion. Contemporary Neurosurgery. 27(8).
  2. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
  3. Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data on file at LifeNet Health, Virginia Beach, VA
Clinical Application
  • Anterior Cervical Discectomy and Fusion
  • VG1 Cervical
  • VertiGraft Fibular Spacer
PreservonDescriptionSize
VG2C-T46P

VG2® Cervical 7° Lordosis

Anterior Height = 6 mm
VG2C-DT7P

VG2 Cervical Large - 7° Lordosis

Anterior Height = 7 mm
VG2C-DR11P

VG2 Cervical Large Parallel

Anterior Height = 11 mm
VG2C-DR10P

VG2 Cervical Large Parallel

Anterior Height = 10 mm
VG2C-DR9P

VG2 Cervical Large Parallel

Anterior Height = 9 mm
VG2C-DR8P

VG2 Cervical Large Parallel

Anterior Height = 8mm
VG2C-DR7P

VG2 Cervical Large Parallel

Anterior Height = 7 mm
VG2C-DR6P

VG2 Cervical Large Parallel

Anterior Height = 6 mm
VG2C-DT11P

VG2 Cervical Large - 7° Lordosis

Anterior Height = 11 mm
VG2C-DT10P

VG2 Cervical Large - 7° Lordosis

Anterior Height = 10 mm
VG2C-DT9P

VG2 Cervical Large - 7° Lordosis

Anterior Height = 9 mm
VG2C-DT8P

VG2 Cervical Large - 7° Lordosis

Anterior Height = 8 mm
VG2C-DT6P

VG2 Cervical Large - 7° Lordosis

Anterior Height = 6 mm
VG2C-T57P

VG2® Cervical 7° Lordosis

Anterior Height = 7 mm
VG2 CPAR11P

VG2® Cervical - Parallel

Anterior Height = 11 mm
VG2 CPAR10P

VG2® Cervical - Parallel

Anterior Height = 10 mm
VG2 CPAR9P

VG2® Cervical - Parallel

Anterior Height = 9 mm
VG2 CPAR8P

VG2® Cervical - Parallel

Anterior Height = 8 mm
VG2 CPAR7P

VG2® Cervical - Parallel

Anterior Height = 7 mm
VG2 CPAR6P

VG2® Cervical - Parallel

Anterior Height = 6 mm
VG2C-T911P

VG2® Cervical 7° Lordosis

Anterior Height = 11mm
VG2C-T810P

VG2® Cervical 7° Lordosis

Anterior Height = 10 mm
VG2C-T79P

VG2® Cervical 7° Lordosis

Anterior Height = 9 mm
VG2C-T68P

VG2® Cervical 7° Lordosis

Anterior Height = 8 mm
VG2C-T1012P

VG2® Cervical 7° Lordosis

Anterior Height = 12 mm
FrozenDescriptionSize
VG2 NCPAR6

VG2® Cervical - Parallel Narrow

Anterior Height = 6 mm
VG2C-T810

VG2® Cervical 7° Lordosis

Anterior Height = 10 mm
VG2 CPAR10

VG2® Cervical Parallel

Anterior Height = 10 mm
VG2 CPAR9

VG2® Cervical Parallel

Anterior Height = 9 mm
VG2 CPAR8

VG2® Cervical Parallel

Anterior Height = 8 mm
VG2 CPAR7

VG2® Cervical Parallel

Anterior Height = 7 mm
VG2 CPAR6

VG2® Cervical Parallel

Anterior Height = 6 mm
VG2C-T911

VG2® Cervical 7° Lordosis

Anterior Height = 11 mm
VG2C-T79

VG2® Cervical 7° Lordosis

Anterior Height = 9 mm
VG2 NCPAR7

VG2® Cervical - Parallel Narrow

Anterior Height = 7 mm
VG2C-T68

VG2® Cervical 7° Lordosis

Anterior Height = 8 mm
VG2C-T57

VG2® Cervical 7° Lordosis

Anterior Height = 7 mm
VG2C-T46

VG2® Cervical 7° Lordosis

Anterior Height = 6 mm
VG2 NCPAR10

VG2® Cervical - Parallel Narrow

Anterior Height = 10 mm
VG2 NCPAR9

VG2® Cervical - Parallel Narrow

Anterior Height = 9 mm
VG2 NCPAR8

VG2® Cervical - Parallel Narrow

Anterior Height = 8 mm
VG2 CPAR11

VG2® Cervical Parallel

Anterior Height = 11 mm
Description
MatriGRAFT® Cloward Dowel,
cylindrical graft with cortical face and cancellous body with pinset on top; processed from distal femoral condyle, proximal tibia, distal tibia or femoral head

 

  • Allows for structural support
  • Allows for impactor to be screwed into graft
  • Allows physician to select appropriate graft for clinical procedure
  • Provides an osteoconductive matrix for incorporation
  • Pre-sized for convenience

Specification Sheets: 

Clinical Application
  • Anterior Cervical and Lumbar Fusion
Freeze-DriedDescriptionSize
CL10

Cloward Dowel

D = 10 mm
CL12

Cloward Dowel

D = 12 mm
M17HS

Cloward Dowel

D = 13 mm
CL 14

Cloward Dowel

D = 14 mm
CL16

Cloward Dowel

D = 16 mm
CL18

Cloward Dowel

D = 18 mm
MR11

Cloward Dowel

D = 11 mm (no set pin hole)
PreservonDescriptionSize
PCL12

Cloward Dowel

D = 12 mm
PCL10

Cloward Dowel

D = 10 mm
PCL11

Cloward Dowel

D = 11 mm (no set pin hole)
PCL13

Cloward Dowell

D = 13 mm
PCL14

Cloward Dowel 

D = 14 mm
PCL16

Cloward Dowel

D = 16 mm
PCL18

Cloward Dowel

D = 18 mm
Description

Designed to provide immediate structural support for Anterior Cervical Discectomy and Fusion (ADCF) procedures

  • Convenience: Pre-sized implants to fit a variety of applications and minimize prep time in the operating room
  • Osteoconductive: Natural osteoconductive scaffold allows for cellular attachment and vascular in-growth
  • 100% Human Bone: Will remodel alongside patient’s own tissue during healing process
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6, without compromising the implant’s inherent osteoconductive properties1
  • Pre-Hydrated, Ambient Storage Available: This implant features Preservon®, a proprietary, glycerol-based preservation technology that allows allograft bio-implants to be stored in a fully hydrated state at ambient temperature. Preservon® eliminates lengthy rehydrating times, and does not require freezer storage2

Specification Sheets: 

 

  1. Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers.
  2. Rodway I, and Gander J. Comparison of Fusion Rates between Glycerol-Preserved and Frozen Composite Allografts in Cervical Fusion. International Scholarly Research Notices. 2014; 2014:960142.
Clinical Application
  • Anterior Cervical Discectomy and Fusion (ACDF)
Freeze-DriedDescriptionSize
TCWP6

Tricortical Cancellous Wedge

H = 6 mm
TCWP7

Tricortical Cancellous Wedge

H = 7 mm
TCWP8

Tricortical Cancellous Wedge

H = 8 mm
TCWP9

Tricortical Cancellous Wedge

H = 9 mm
TCWP10

Tricortical Cancellous Wedge

H = 10 mm
TCWP11

Tricortical Cancellous Wedge

H = 11 mm
TCWP12

Tricortical Cancellous Wedge

H = 12 mm
TCWP5

Tricortical Cancellous Wedge

H = 5 mm
PreservonDescriptionSize
PTCWP5

Tricortical Cancellous Wedge

H = 5 mm
PTCWP6

Tricortical Cancellous Wedge

H = 6 mm
PTCWP7

Tricortical Cancellous Wedge

H = 7 mm
PTCWP8

Tricortical Cancellous Wedge

H = 8 mm
PTCWP9

Tricortical Cancellous Wedge

H = 9 mm
PTCWP10

Tricortical Cancellous Wedge

H = 10 mm
PTCWP11

Tricortical Cancellous Wedge

H = 11 mm
PTCWP12

Tricortical Cancellous Wedge

H = 12 mm
Description

MatriGRAFT® Unicortical Cancellous Spacer  is a  precision cut cancellous block with a single cortical face recovered from femoral condyles, femoral heads, distal tibia, and the talus

  • Allows for sturctural support with single cortical face
  • Allows physician to select appropriate graft for clinical procedure
  • Provides and osteoconductive matrix for incorporation
  • Pre-sized for convenience

Specification Sheets: 

Clinical Application
  • Anterior Cervical Fusion

Tricortical Cancellous Wedge-Parallel, Iliac Crest Wedge

Measurements

L = 11 mm and W = 14 mm

Freeze-DriedDescriptionSize
CCSPR5

Unicortical Cancellous Spacer

H = 5 mm
CCSPR6

Unicortical Cancellous Spacer

H = 6 mm
CCSPR7

Unicortical Cancellous Spacer

H = 7 mm
CCSPR8

Unicortical Cancellous Spacer

H = 8 mm
CCSPR9

Unicortical Cancellous Spacer

H = 9 mm
CCSPR10

Unicortical Cancellous Spacer

H = 10 mm
28103_vertigraft_vg1lam_specsheet.pdf
Description
Solid, one piece cortical construct designed to provide biomechanical strength, predictable decompression and lamina reconstruction for Laminoplasty procedures
• Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6, without compromising the implant’s inherent osteoconductive properties1
 
• Fully hydrated, Ambient Storage: Vertigraft Allograft VG1 features Preservon®, a proprietary, glycerol-based preservation technology that allows allograft bio-implants to be stored in a fully hydrated state at ambient temperature. Preservon eliminates lengthy rehydrating times, and does not require freezer storage2
 
• Solid asymmetrical design optimizes bone and graft contact area of the resected lateral mass and lamina
 
• Size specific allografts maximize fit and fill options to accommodate the appropriate amount of decompression needed
 
  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
  2. Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data on file at LifeNet Health, Virginia Beach, VA.
Clinical Application
  • Posterior Cervical Laminoplasty, for use with DePuy Synthes ARCH™ Fixation System
PreservonDescriptionSize
VG1 LAM4B

Laminoplasty Spacer

L = 12mm, H = 6mm, W = 9mm
VG1 LAM6B

Laminoplasty Spacer

L = 12mm, H = 6mm, W = 9mm
VG1 LAM8B

Laminoplasty Spacer

L = 12mm, H = 6mm, W = 9mm
VG1 LAM10B

Laminoplasty Spacer

L = 10mm, H = 6mm, W = 9mm
VG1 LAM12B

Laminoplasty Spacer

L = 12mm, H = 6mm, W = 9mm
68-60-030-01.pdf
Description
Tricortical iliac crest wedge, designed to provide immediate structural support and restore segmental bone loss
  • Osteoconductive: Natural bone matrix facilitates cell attachment and proliferation, and vascular in-growth
  • Structural: Tricortical plate provides immediate structural support
  • 100% Human Bone: Can remodel with the patient’s own tissue during the healing process
  • Pre-Hydrated: Allograft bio-implants featuring Preservon® are stored in a fully-hydrated state at ambient temperatures. Preservon eliminates thawing and re-hydration time and does not require freezer storage or compromise the graft’s inherent osteoconductive properties1
  • Sterile: Sterilized using patented and proprietary Allowash XG® technology which provides a sterility assurance level (SAL) of 10-6, without compromising the graft’s inherent osteoconductive properties2
  • Convenient: Implant is pre-sized to fit a variety of applications and minimize prep time in the operating room
  1. Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data of file at LifeNet Health. 
  2. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG.” 2007 Bio-Implants Brief
Clinical Application
  • High Tibial Osteotomies
  • Pelvic Osteotomies
  • Foot & Ankle Osteotomies
  • Fracture Management
  • Glenoid Reconstruction
  • Anterior Cervical Discectomy and Fusion
  • Corpectomy
PreservonDescriptionSize
PICW0.6

Iliac Crest Wedge

H = 6 mm
PICW0.7

Iliac Crest Wedge

H = 7 mm
PICW0.8

Iliac Crest Wedge

H = 8 mm
PICW0.9

Iliac Crest Wedge

H = 9 mm
PICW1

Iliac Crest Wedge

H = 10 mm
PICW2

Iliac Crest Wedge

H = 12 mm
PICW5

Iliac Crest Wedge

H = 15 mm
PICW8

Iliac Crest Wedge

H = 18 mm
PICWS

Iliac Crest Wedge

H = 20 mm
PICW2.5

Iliac Crest Wedge

H = 25 mm
Freeze-DriedDescriptionSize
ICW0.6

Iliac Crest Wedge

H = 6 mm
ICW0.7

Iliac Crest Wedge

H = 7 mm
ICW0.8

Iliac Crest Wedge

H = 8 mm
ICW0.9

Iliac Crest Wedge

H = 9 mm
ICW1

Iliac Crest Wedge

H = 10 mm
ICW2

Iliac Crest Wedge

H = 12 mm
ICW8

Iliac Crest Wedge

H = 18 mm
ICWS

Iliac Crest Wedge

H = 20 mm
ICW2.5

Iliac Crest Wedge

H = 25 mm
Description

Bio-Implant designed with two cortical endplates supporting a cancellous center for ACDF Procedures.

  • Proven Clinical Performance: The cortical cancellous design optimizes strength and clinical success. A prospective study found 100% fusion rates after 12 months in 74 ACDF Patients.1
  • Osteoconductive: Large cancellous matrix facilitates bone growth and remodeling in accordance with Wolff’s Law.
  • Stability: Textured surface and multiple footprints optimize fit and fill while reducing migration.
  • Sagittal Balance: Available in both neutral and lordotic footprints to reproduce and correct the anatomy.
  • Convenience: Preservon® is a proprietary, glycerol-based preservation technology that allows LifeNet Health allograft implants to be stored in a fully hydrated state at ambient temperature. Lengthy thawing or rehydration time is eliminated with out compromising allograft strength.2
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6, without compromising the implants inherent osteoconductive properties.3

Specification Sheets: 

 
References:
1. Abla A, El Kadi H, Bost J, Maroon J, and Wert M. Allograft Composite Cortical and Cancellous Bone Graft for Anterior Cervical Fusion. Contemporary Neurosurgery: A Biweekly Publication for Clinical Neurosurgical Continuing Medical Education. 2005;27(8):1-6.
2. Independent sources include Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data on File at LifeNet Health, Virginia Beach VA.
3. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG” 2007 BioImplants Brief
VG2® Cervical Allograft Spacer and VG1® Cervical Allograft Spacer
68-60-019-01.pdf
Description

A natural mix of cortical and cancellous bone chips designed to encourage bi-phasic remodeling

  • Osteoconductive: Natural bone matrix facilitates cell attachment and proliferation, and vascular in-growth
  • Bi-Phasic: Natural mix of cortical and cancellous bone facilitates bi-phasic remodeling
  • Pre-hydrated: Allograft bio-implants featuring Preservon® are stored in a fully-hydrated state at ambient temperatures. Preservon eliminates thawing and re-hydration time, does not require freezer storage, and does not compromise the graft’s inherent osteoconductive properties1
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology which provides a sterility assurance level of 10-6, without compromising the graft’s inherent osteoconductive properties2
  • Versatile: Available in grind sizes of 1-4 mm or 1-8 mm in multiple volumes to meet surgical needs
  • Absorbent: Absorbs and retains bioactive fluids like blood, platelet rich plasma (PRP), and bone marrow aspirate (BMA)

 

  1. Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data of file at LifeNet Health.
  2. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
Clinical Application
  • Any surgical application that requires bone void filler 
  • ReadiGraft Cancellous Chips
  • MatriGraft Femoral Head (Grinder)
Freeze-DriedDescriptionSize
CC10

Cortical/Cancellous, 1 - 8 mm

10 cc
CC1/4

Cortical/Cancellous, 1 - 8 mm

20 cc
CC30

Cortical/Cancellous, 1 - 8 mm

30 cc
CC1/2

Cortical/Cancellous, 1 - 8 mm

40 cc
CC60

Cortical/Cancellous, 1 - 8 mm

60 cc
CC90

Cortical/Cancellous, 1 - 8 mm

90 cc
PreservonDescriptionSize
PCC15 14

Cortical/Cancellous, 1 - 4 mm

15 cc
PCC30 14

Cortical/Cancellous, 1 - 4 mm

30 cc
PCC60 14

Cortical/Cancellous, 1 - 4 mm

60 cc
PCC90 14

Cortical/Cancellous, 1 -4 mm

90 cc
PCC10

Cortical/Cancellous, 1 - 8 mm

10 cc
PCC15

Cortical/Cancellous, 1 - 8 mm

15 cc
PCC1/4

 Cortical/Cancellous, 1 - 8 mm

20 cc
PCC30

Cortical/Cancellous, 1 - 8 mm

30 cc
PCC1/2

Cortical/Cancellous, 1 - 8 mm

40 cc
PCC60

Cortical/Cancellous, 1 - 8 mm

60 cc
PCC90

Cortical/Cancellous, 1 - 8 mm

90 cc
68-60-135.pdf
Description
I/C Graft Chamber is a proprietary mix of demineralized bone material and cancellous chips designed to maintain osteoinductive potential and osteoconductive properties
  • Allows surgeons to customize hydration options to fit patients’ needs by using bone marrow aspirate (BMA), Platelet Rich Plasma (PRP), Whole Blood, or Saline
  • When combined with bone marrow aspirate, the I/C Graft Chamber provides the three necessary mechanisms for bone formation (Osteoconductivity, Osteoinductive Potential and Osteogenicity)
  • Comprised of 100% natural bone matrix which is remodeled naturally during the bone healing process
  • Contains no fillers or carriers commonly used in bone putties and gels
  • The natural porous structure of cancellous chips provides an optimal scaffold for cellular attachment and vascular in-growth
Clinical Application
  • Utilized as a bone void filler or graft extender during spinal fusion surgeries to promote the likelihood of fusion
  • Used to fill the cavities in and around interbody spacers or serve as scaffold across lateral gutters bridging the transverse processes
Freeze-DriedDescriptionSize
GDS005T

DBM Particulate

5 cc
GDS005T

DBM Particulate

5 cc
GDS010T

DBM Particulate

10 cc
GDS010T

DBM Particulate

10 cc
GDS015T

DBM Particulate

15 cc
GDS015T

DBM Particulate

15 cc
68-60-023-01.pdf
Description

Demineralized bone chips and particulates designed to promote bone healing in patients with a high risk of non-union

  • Osteoinductive Potential: Demineralized using proprietary PAD® technology that targets optimal residual calcium levels of 1-4% without compromising the grafts inherent osteoconductive properties or osteoinductive potential1-4
  • Osteoconductive: Natural bone matrix facilitates cell attachment and proliferation, and vascular in-growth 
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology which provides a sterility assurance level of 10-6, without compromising the graft’s inherent osteoconductive properties5
  • Versatile: Available in multiple sizes and volumes to meet surgical needs
  •  
  • Absorbent: Absorbs and retains bioactive fluids like blood, platelet rich plasma (PRP), and bone marrow aspirate (BMA)

 

  1. Zhang M, Powers R, Wolfinbarger L. (1997). Effect(s) of demineralization process on the osteoinductivity of demineralized bone matrix. J Periodontol, 68:1085-1092. 
  2. Turonis JW, McPherson JC 3rd, Cuening MF. (2006). The affects of residual calcium in decalcified freeze-dried bone allograft in a critical-sized defect in the Rattus norvegicus calvarium. J Oral Implantol. 32(2), 55-62. 
  3. Herold RW, Pashley DH, Cuening MF. (2002). Effects of varying degrees of allograft decalcification on the cultured porcine osteoclast cells. J Periodontol, 72(2), 213-219. 
  4. Mott DA, Mailhot J, Cuenin MF, Sharawy M, Borke J. (2002). Enhancement of osteoblast proliferation in vitro by selective enrichment of demineralized freeze-dried bone allograft with specific growth factors. J Oral Implantiol, 28(2), 57-66. 
  5. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
Clinical Application
  • Any surgical application that requires bone void filler
Freeze-DriedDescriptionSize
DCAN40

Demineralized Cancellous Chips 1 - 4 mm

40 cc
68-60-023-01.pdf
Description

Demineralized bone chips and particulates designed to promote bone healing in patients with a high risk of non-union

  • Osteoinductive Potential: Demineralized using proprietary PAD® technology that targets optimal residual calcium levels of 1-4% without compromising the grafts inherent osteoconductive properties or osteoinductive potential1-4
  • Osteoconductive: Natural bone matrix facilitates cell attachment and proliferation, and vascular in-growth 
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology which provides a sterility assurance level of 10-6, without compromising the graft’s inherent osteoconductive properties5
  • Versatile: Available in multiple sizes and volumes to meet surgical needs
  •  
  • Absorbent: Absorbs and retains bioactive fluids like blood, platelet rich plasma (PRP), and bone marrow aspirate (BMA)

 

  1. Zhang M, Powers R, Wolfinbarger L. (1997). Effect(s) of demineralization process on the osteoinductivity of demineralized bone matrix. J Periodontol, 68:1085-1092. 
  2. Turonis JW, McPherson JC 3rd, Cuening MF. (2006). The affects of residual calcium in decalcified freeze-dried bone allograft in a critical-sized defect in the Rattus norvegicus calvarium. J Oral Implantol. 32(2), 55-62. 
  3. Herold RW, Pashley DH, Cuening MF. (2002). Effects of varying degrees of allograft decalcification on the cultured porcine osteoclast cells. J Periodontol, 72(2), 213-219. 
  4. Mott DA, Mailhot J, Cuenin MF, Sharawy M, Borke J. (2002). Enhancement of osteoblast proliferation in vitro by selective enrichment of demineralized freeze-dried bone allograft with specific growth factors. J Oral Implantiol, 28(2), 57-66. 
  5. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
Clinical Application
  • Any surgical application that requires bone void filler
Freeze-DriedDescriptionSize
DGC40

Demineralized Cortical Chips 125 - 1000 microns

40 cc
DGC20

Demineralized Cortical Chips 125 - 1000 microns

20 cc
Description

ReadiGRAFT® Fascia Lata is a fibrous covering of muscle recovered from the lateral aspect of the thigh

  • Allows physician to use for various clinical application
Clinical Application
  • Dural replacement
  • Blepharoplasty (Drooped Eyelid Repair)

For Duraplasty: Pericardium

Achilles Tendon, Patellar Ligament, Tibial Tendons, Semitendinosus, Gracilis

Freeze-DriedDescriptionSize
FL Strip

Strip

3 x 150 mm (2/pkg)
FL S

Small

30 x 60 mm
FL M

Medium

30 x 150 mm
FL L

Large

80 x 200 mm
Description

ReadiGRAFT® Pericardium is a sac-like membrane surrounding the heart

  • Allows physician to use for various clinical applications
Clinical Application
  • Dural replacement/repair
  • Sceral substitute

Fascia Lata

Freeze-DriedDescriptionSize
PERI 1.5

Pericardium

15 x 15 mm
PERI S

Small

20 x 40 mm
PERI M

Medium

40 x 40 mm
PERI L

Large

60 x 60 mm
Description

Optium® DBM Putty is designed to set the standard for safety, quality and performance in DBM technology

  • Demineralized using LifeNet Health's patented and proprietary PAD® process which exposes natural growth factors trapped within cortical bone
  • Every lot of final product is tested for osteoinductive potential
  • Fibers provide a natural architecture with increased surface area to encourage cellular attachment
  • LifeNet Health's patented Allowash XG® technology provides a sterility assurance level of 10-6
  • Optium's carrier, glycerol, gives it an extensive, published clinical history and proven safe and effective in bone void filling applications
  • Ready to use
  • Available in different volumes

Specification Sheets: 

Clinical Application
  • Joint Reconstruction and Revision
  • Trauma
  • Spine

I/C Graft Chamber® and Optium® DBM Gel

Freeze-DriedDescriptionSize
TPUT01

Putty (DBM Fibers & Glycerol)

1 cc
TPUT02

Putty (DBM Fibers & Glycerol)

2.5 cc
TPUT05

Putty (DBM Fibers & Glycerol)

5 cc
TPUT10

Putty (DBM Fibers & Glycerol)

10 cc
Description

Optium® DBM Gel is designed to set the standard for safety, quality, and performance in DBM technology

  • Demineralized using LifeNet Health's patented and proprietary PAD® process which exposes natural growth factors trapped within cortical bone
  • Every lot of final product is tested for osteoinductive potential 
  • Fibers provide a natural architecture with increased surface area to encourage cellular attachment
  • LifeNet Health's patented Allowash XG® technology provides a sterility assurance level of 10-6
  • Optium's carrier, glycerol, gives it an extensive, published clinical history and proven safe and effective in bone void filling applications
  • Ready to use
  • Available in different volumes

Specification Sheets: 

Clinical Application
  • Joint Reconstruction and Revision
  • Trauma
  • Spine
Freeze-DriedDescriptionSize
TGEL01

Gel (Particulate DBM & Glycerol)

1 cc
TGEL05

Gel (Particulate DBM & Glycerol)

5 cc
TGEL10

Gel (Particulte DBM & Glycerol)

10 cc
68-60-023-01.pdf
Description

Demineralized bone chips and particulates designed to promote bone healing in patients with a high risk of non-union

  • Osteoinductive Potential: Demineralized using proprietary PAD® technology that targets optimal residual calcium levels of 1-4% without compromising the grafts inherent osteoconductive properties or osteoinductive potential1-4
  • Osteoconductive: Natural bone matrix facilitates cell attachment and proliferation, and vascular in-growth 
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology which provides a sterility assurance level of 10-6, without compromising the graft’s inherent osteoconductive properties5
  • Versatile: Available in multiple sizes and volumes to meet surgical needs
  •  
  • Absorbent: Absorbs and retains bioactive fluids like blood, platelet rich plasma (PRP), and bone marrow aspirate (BMA)

 

  1. Zhang M, Powers R, Wolfinbarger L. (1997). Effect(s) of demineralization process on the osteoinductivity of demineralized bone matrix. J Periodontol, 68:1085-1092. 
  2. Turonis JW, McPherson JC 3rd, Cuening MF. (2006). The affects of residual calcium in decalcified freeze-dried bone allograft in a critical-sized defect in the Rattus norvegicus calvarium. J Oral Implantol. 32(2), 55-62. 
  3. Herold RW, Pashley DH, Cuening MF. (2002). Effects of varying degrees of allograft decalcification on the cultured porcine osteoclast cells. J Periodontol, 72(2), 213-219. 
  4. Mott DA, Mailhot J, Cuenin MF, Sharawy M, Borke J. (2002). Enhancement of osteoblast proliferation in vitro by selective enrichment of demineralized freeze-dried bone allograft with specific growth factors. J Oral Implantiol, 28(2), 57-66. 
  5. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
Clinical Application
  • Any surgical application that requires bone void filler
Freeze-DriedDescriptionSize
DCC1/4

Demineralized Cortical/Cancellous

20 cc
Description

ReadiGraft BLX Fibers are a proprietary mix of demineralized cortical fibers and mineralized cancellous
chips specifically engineered to maintain the osteoinductive potential and osteoconductive properties
of the graft while providing surgeons with the operative flexibility to customize hydrating options to fit
patient’s needs.

  • International use only, not available in all markets
  • Osteoconductive: The natural osteoconductive porous architecture of cancellous bone and the increased surface area of demineralized cortical fibers provides a scaffold for cellular attachment and proliferation
  • Osteoinductive Potential: The cortical fibers are demineralized using LifeNet Health’s patented and proprietary PAD® technology. This technology carefully exposes natural growth factors trapped within cortical bone while maintaining its inherent osteoinductive potential.
  • No Carrier: Contains no fillers or carriers commonly used in bone putties and gels
  • Customizable Hydration: Allows surgeons to customize hydration options to fit patient’s needs by the following hydration options:
    • Platelet Rich Plasma (PRP)
    • Bone Marrow Aspirate (BMA)
    • Whole Blood
    • Saline
    • Antibiotic Solution
  • Biocompatible: ReadiGraft BLX DBM Fibers are comprised of 100% natural bone matrix which is remodeled naturally during the bone healing process
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6, without compromising the implant’s inherent osteoconductivity or osteoinductive potential.

Specification Sheet: 

Clinical Application
  • Any surgical application that requires bone void filler

Freeze-DriedDescriptionSize
DF-1002

BLX DBM Fibers

2 cc
DF-1003

BLX DBM Fibers

5 cc
DF-1004

BLX DBM Fibers

15 cc
DF-1005

BLX DBM Fibers

30 cc
DF-1006

BLX DBM Fibers

10 cc
68-60-021-01.pdf
Description

Sterile cancellous chips that provide a natural osteoconductive matrix to encourage bone healing

  • Osteoconductive: Natural bone matrix facilitates cell attachment and proliferation, and vascular in-growth
  • Pre-hydrated: Allograft bio-implants featuring Preservon® are stored in a fully-hydrated state at ambient temperatures. Preservon eliminates thawing and re-hydration time, does not require freezer storage, and does not compromise the graft’s inherent osteoconductive properties1
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology which provides a sterility assurance level of 10-6, without compromising the graft’s inherent osteoconductive properties2
  • Versatile: Available in multiple grind sizes and volumes to meet surgical needs
  • Absorbent: Absorbs and retains bioactive fluids like blood, platelet rich plasma (PRP), and bone marrow aspirate (BMA)

 

  1. Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data of file at LifeNet Health. 
  2. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief
Clinical Application
  • Any surgical application that requires bone void filler
  • ReadiGraft Cancellous Cubes
  • ReadiGraft Cortical/Cancellous Chips
  • MatriGraft Femoral Head (Grinder)
Freeze-DriedDescriptionSize
CAN15 14BP

Crushed Cancellous Chips, 1 - 4 mm

15 cc
CAN20 14BP

Crushed Cancellous Chips, 1 - 4 mm

20 cc
CAN30 14BP

Crushed Cancellous Chips, 1 - 4 mm

30 cc
CAN40 14BP

Crushed Cancellous Chips, 1 - 4 mm

40 cc
CAN60 14BP

Crushed Cancellous Chips, 1 - 4 mm

60 cc
CAN80 14BP

Crushed Cancellous Chips, 1 - 4 mm

80 cc
CAN90 14BP

Crushed Cancellous Chips, 1 - 4 mm

90 cc
CAN10

Crushed Cancellous Chips, 1 - 8 mm

10 cc
CAN15

Crushed Cancellous Chips, 1 - 8 mm

15 cc
CAN1/4

Crushed Cancellous Chips, 1 - 8 mm

20 cc
CAN30

Crushed Cancellous Chips, 1 - 8 mm

30 cc
CAN1/2

Crushed Cancellous Chips, 1 - 8 mm

40 cc
CAN60

Crushed Cancellous Chips, 1 - 8 mm

60 cc
CAN1

Crushed Cancellous Chips, 1 - 8 mm

80 cc
CAN90

Crushed Cancellous Chips, 1 - 8 mm

90 cc
CAN90 410BP

Crushed Cancellous Chips, 4 - 10 mm

90 cc
CAN60 410BP

Crushed Cancellous Chips, 4 - 10 mm

60 cc
CAN30 410BP

Crushed Cancellous Chips, 4 - 10 mm

30 cc
CAN15 410BP

Crushed Cancellous Chips, 4 - 10 mm

15 cc
CAN5

Crushed Cancellous Chips, 1 - 8 mm

5 cc
FrozenDescriptionSize
FCAN90 14

Crushed Cancellous Chips, 1 - 4 mm

90 cc
FCAN60 14

Crushed Cancellous Chips, 1 - 4 mm

60 cc
FCAN15 410

Crushed Cancellous Chips, 4 - 10 mm

15 cc
FCAN30 410

Crushed Cancellous Chips, 4 - 10 mm

30 cc
FCAN90 410

Crushed Cancellous Chips, 4 - 10 mm

90 cc
FCAN60 410

Crushed Cancellous Chips, 4 - 10 mm

60 cc
FCAN30 14

Crushed Cancellous Chips, 1 - 4 mm

30 cc
FCAN15 14

Crushed Cancellous Chips, 1 - 4 mm

15 cc
FCAN1/2

Crushed Cancellous Chips, 1 - 8 mm

40 cc
FCAN30

Crushed Cancellous Chips, 1 - 8 mm

30 cc
FCAN1

Crushed Cancellous Chips, 1 - 8 mm

80 cc
FCAN90

Crushed Cancellous Chips, 1 - 8 mm

90 cc
FCAN2

Crushed Cancellous Chips, 1 - 8 mm

160 cc
FCAN1/4

Crushed Cancellous Chips, 1 - 8 mm

20 cc
PreservonDescriptionSize
PCAN60

Crushed Cancellous Chips, 1 - 8 mm

60 cc
PCAN1/2

Crushed Cancelleous Chips, 1 - 8 mm

40 cc
PCAN20 14

Crushed Cancellous Chips, 1 - 4 mm

20 cc
PCAN30 14

Crushed Cancellous Chips, 1 - 4 mm

30 cc
PCAN40 14

Crushed Cancellous Chips, 1 - 4 mm

40 cc
PCAN15 14

Crushed Cancellous Chips, 1 - 4 mm

15 cc
PCAN90

Crushed Cancelleous Chips, 1 - 8 mm

90 cc
PCAN1/4

Crushed Cancelleous Chips, 1 - 8 mm

20 cc
PCAN30

Crushed Cancelleous Chips, 1 - 8 mm

30 cc
PCAN60 14

Crushed Cancellous Chips, 1 - 4 mm

60 cc
PCAN10

Crushed Cancellous Chips, 1 - 8 mm

10 cc
PCAN80 14

Crushed Cancellous Chips, 1 - 4 mm

80 cc
PCAN30 410

Crushed Cancellous Chips, 4 - 10 mm

30 cc
PCAN60 410

Crushed Cancellous Chips, 4 - 10 mm

60 cc
PCAN90 410

Crushed Cancellous Chips, 4 - 10 mm

90 cc
PCAN15 410

Crushed Cancellous Chips, 4 - 10 mm

15 cc
PCAN1

Crushed Cancellous Chips, 1- 8 mm

80 cc
PCAN90 14

Crushed Cancellous Chips, 1 - 4 mm

90 cc
PCAN5

Crushed Cancellous Chips, 1 - 8 mm

5 cc
PCAN15

Crushed Cancelleous Chips, 1 - 8 mm

15 cc
Description
PliaFX Strip is composed of 100% cortical bone fibers, demineralized to encourage bone formation and patient healing. When rehydrated with blood or bone marrow aspirate, the PliaFX Strip remains intact and is flexible to conform to the implant site
 
• Osteoinductive Potential: Optimally demineralized by LifeNet Health’s patented and proprietary PAD® technology to expose natural growth factors1-5
• Osteoconductive: Provides a scaffold with specific pore size and porosity to promote cellular attachment and proliferation6
• 100% Cortical Bone: Facilitates natural remodeling during the bone healing process (no human or synthetic carriers)
• Resists Migration: Pre-formed to remain intact and in place
• Versatile: Customizable and flexible upon rehydration to conform to the implant site
• Safety: Terminally sterilized using proprietary and patented Allowash XG® technology, providing a sterility assurance level of 10-6 to reduce the risk of disease transmission
• Convenience: Ambient storage for up to 5 years
 
Specification Sheet: 
Clinical Application
• Posterolateral Fusion
• Posterior Cervical Fusion
• Any surgical application that requires bone void filler

References:

1. Zhang M, Powers RM, and Wolfinbarger L. Effect(s) of the demineralization process on the osteoinductivity of demineralized bone matrix. J Periodontol. 1997; 68:1085-1092
2. Turonis JW, McPherson JC 3rd, Cuenin MF, et al. The effect of residual calcium in decalcified freeze-dried bone allograft in a critical-sized defect in the Rattus norvegicus calvarium. J Oral Implantol. 2006; 32(2):55-62
3. Herold RW, Pashley DH, Cuenin MF, et al. The effects of Varying degrees of Allograft Decalcification on Cultured Porcine Osteoclast cells. J Periodontol. 2002 Feb; 73(2):213-9
4. Mott DA, Mailhot J, Cuenin MF, et al. Enhancement of osteoblast proliferation in vitro by selective enrichment of demineralized freeze-dried bone allograft with specific growth factors. J Oral Implantol. 2002; 28(2):57-66
5. Pietrzak WS, Ali SN, Chitturi D, et al. BMP depletion occurs during prolonged acid demineralization of bone: characterization and implications for graft preparation. Cell Tiss. Bank. 2007 (Published on line)
6. Data on file at LifeNet Health, DHF 14-006
Room TemperatureDescriptionSize
BL-1700-25100

Order Code

length 100 mm, width 25 mm, thickness 4 mm
BL-1700-25050

Order Code

length 50 mm, width 25 mm, thickness 4 mm
68-60-053-01.pdf
Description

Solid, one piece cortical implant designed to provide biomechanical strength for ALIF procedures

  • Solid, one piece cortical construction designed to provide biomechanical strength
  • Central void allows for physician preferred osteoinductive filler
  • Chamfered posterior surface and bulleted nose for ease of insertion
  • Stability: Textured surface designed to reduce migration
  • Variety: Multiple footprints in both parallel and lordotic configurations to better match patient anatomy
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1
  • Fully Hydrated, Ambient Storage Available: This implant features Preservon® , a proprietary, glycerol-based preservation technology that allows allograft bio-implants to be stored in a fully hydrated state at ambient temperature. Preservon eliminates lengthy thawing and rehydrating times, and does not require freezer storage2

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
  2.  Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data on file at LifeNet Health, Virginia Beach, VA

 

Clinical Application
  • Anterior Lumbar Interbody Fusion
  • VG2 TLIF - for Transforaminal Lumbar Interbody Fusion
  • VG2 PLIF - for Posterior Lumbar Interbody Fusion
  • VG2 RAMP - for Posterior Lumbar Interbody Fusion
FrozenDescriptionSize
VG1B-10A

VG1® ALIF Anterior - 5° Lordosis

Anterior Height = 10.75 mm
VG1B-12A

VG1® ALIF Anterior - 5° Lordosis

Anterior Height = 12.75 mm
VG1B-14A

VG1® ALIF Anterior - 5° Lordosis

Anterior Height = 14.75 mm
VG1B-16A

VG1® ALIF Anterior - 5° Lordosis

Anterior Height = 16.75 mm
VG1B-18A

VG1® ALIF Anterior - 5° Lordosis

Anterior Height = 18.75 mm
VG1B-20A

VG1® ALIF Anterior - 5° Lordosis

Anterior Height = 20.75 mm
VG1B-10AL

VG1® ALIF Anterior Lateral - 5° Lordosis

Anterior Height = 10.75 mm
VG1B-12AL

VG1® ALIF Anterior Lateral - 5° Lordosis

Anterior Height = 12.75 mm
VG1B-14AL

VG1® ALIF Anterior Lateral - 5° Lordosis

Anterior Height = 14.75 mm
VG1B-16AL

VG1® ALIF Anterior Lateral - 5° Lordosis

Anterior Height = 16.75 mm
VG1B-18AL

VG1® ALIF Anterior Lateral - 5° Lordosis

Anterior Height = 18.75 mm
VG1B-20AL

VG1® ALIF Anterior Lateral - 5° Lordosis

Anterior Lateral = 20.75 mm
Freeze-DriedDescriptionSize
VG1B-10ALBP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 10.75 mm
VG1B-12ALBP

VG1® ALIF- Anterior Lateral - 5° Lordosis 

Anterior Height = 12.75 mm
VG1B-14ALBP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 14.75 mm
VG1B-16ALBP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 16.75 mm
VG1B-18ALBP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 18.75
VG1B-20ALBP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 20.75
PreservonDescriptionSize
VG1B-10AP

VG1® ALIF- Anterior - 5° Lordosis

Anterior Height = 10.75 mm
VG1B-18ALP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 18.75 mm
VG1B-18HAP

VG1® ALIF Anterior - 10° Lordosis

Anterior Height = 18.75 mm
VG1B-16HAP

VG1® ALIF Anterior - 10° Lordosis

Anterior Height = 16.75 mm
VG1B-14HAP

VG1® ALIF Anterior - 10° Lordosis

Anterior Height = 14.75 mm
VG1B-12HAP

VG1® ALIF Anterior - 10° Lordosis

Anterior Height = 12.75 mm
VG1B-10HAP

VG1® ALIF Anterior - 10° Lordosis

Anterior Height = 10.75 mm
VG1B-20ALP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 20.75 mm
VG1B-16ALP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 16.75 mm
VG1B-12AP

VG1® ALIF- Anterior - 5° Lordosis

Anterior Height = 12.75 mm
VG1B-14ALP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 14.75 mm
VG1B-12ALP

VG1® ALIF- Anterior Lateral - 5° Lordosis

Anterior Height = 12.75 mm
VG1B-10ALP

VG1® ALIF-Anterior Lateral - 5° Lordosis

Anterior Height = 10.75 mm
VG1B-20AP

VG1® ALIF- Anterior - 5° Lordosis

Anterior Height = 20.75
VG1B-18AP

VG1® ALIF- Anterior - 5° Lordosis

Anterior Height = 18.75 mm
VG1B-16AP

VG1® ALIF- Anterior - 5° Lordosis

Anterior Height = 16.75 mm
VG1B-14AP

VG1® ALIF- Anterior - 5° Lordosis

Anterior Height = 14.75
VG1B-20HAP

VG1® ALIF Anterior - 10° Lordosis

Anterior Height = 20.75 mm
68-60-128.pdf
Description

Solid one piece cortical spacer designed to provide biomechanical strength for spinal fusion inter-body and discectomy procedures

  • Strength: Cortical Construction
  • Stability: Textured surface area to reduce migration
  • Variety: Multiple footprints in both parallel and lordotic configurations to better match patient anatomy
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1
  • Convenience: Freeze-dried for room temperature storage

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
Clinical Application

Spinal fusion inter-body and discectomy procedures

Freeze-DriedDescriptionSize
VHUMCS8

Humeral Spacer Parallel

Anterior Height = 8 mm
VHUMCS10

Humeral Spacer Parallel

Anterior Height = 10 mm
VHUMCS12

Humeral Spacer Parallel

Anterior Height = 12 mm
VHUMCS14

Humeral Spacer Parallel

Anterior Height = 14 mm
VHUMCS16

Humeral Spacer Parallel

Anterior Height = 16 mm
VHUMW11

Humeral Spacer Lordotic

Anterior Height = 14 mm
VHUMW13

Humeral Spacer Lordotic

Anterior Height = 16 mm
VHUMW15

Humeral Spacer Lordotic

Anterior Height = 18 mm
VHUMW17

Humeral Spacer Lordotic

Anterior Height = 20 mm
Description

Bio-implant designed with two cortical endplates supporting a cancellous center for PLIF procedures

  • Osteoconductive: Large cancellous core facilitates early bone growth
  • Stability: Textured surface designed to reduce migration
  • Variety: Multiple footprints in both parallel and lordotic configurations to better match patient anatomy
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1
  • Uniform dimensions

Specification Sheet: 

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
Clinical Application
  • • Posterior Lumbar Interbody Fusion
  • VG2 TLIF - for Transforaminal Lumbar Interbody Fusion
  • VG1 ALIF - for Anterior Lumbar Body Fusion
  • VG2 RAMP - for Posterior Lumbar Interbody Fusion
FrozenDescriptionSize
VG2P-P9

VG2® PLIF Parallel

Anterior Height = 9 mm
VG2P-P11

VG2® PLIF Parallel

Anterior Height = 11 mm
VG2P-P11N

VG2® PLIF Parallel

Anterior Height = 11 mm
VG2P-P13

VG2® PLIF Parallel

Anterior Height = 13 mm
VG2P-P13N

VG2® PLIF Parallel

Anterior Height = 13 mm
VG2P-T57

VG2® PLIF Lordotic

Anterior Height = 7 mm
VG2P-T79

VG2® PLIF Lordotic

Anterior Height = 9 mm
VG2P-T911N

VG2® PLIF Lordotic

Anterior Height = 11 mm
VG2P-T911W

VG2® PLIF Lordotic

Anterior Height = 11 mm
VG2P-T1113N

VG2® PLIF Lordotic

Anterior Height = 13 mm
VG2P-T1113W

VG2® PLIF Lordotic

Anterior Height = 13 mm
68-60-055-01.pdf
Description

All cortical bio-implant designed to restore disc height and sagittal alignment as an alternative allograft for PLIF procedures

  • Size- specific allografts for selection of exact size implant for each procedure 
  • Stability: Textured surface designed to reduce migration
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1
  • Uniform dimensions

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization UsingAllowash XG®.” 2007 Bio-Implants Brief.
Clinical Application

• Posterior Lumbar Interbody Fusion

  • VG2 TLIF - for Transforaminal Lumbar Interbody Fusion
  • VG2 PLIF - for Posterior Lumbar Interbody Fusion
  • VG1 ALIF - for Anterior Lumbar Body Fusion
FrozenDescriptionSize
VG2 RAMP911

VG2® Trapezoid Ramp

Anterior Height = 11 mm
VG2 RAMP913

VG2® Trapezoid Ramp

Anterior Height = 13 mm
VG2 RAMP1113

VG2® Trapezoid Ramp

Anterior Height = 13 mm
68-60-056-01.pdf
Description

Bio-implant designed with two cortical endplates supporting a cancellous center for TLIF procedures

  • Osteoconductive: Large cancellous core facilitates early bone growth
  • Stability: Textured surface designed to reduce migration
  • Variety: Multiple footprints in both parallel and lordotic configurations to better match patient anatomy
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1
  • Uniform dimensions

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief
Clinical Application
  • Transforaminal Lumbar Interbody Fusion
  • VG2 PLIF - for Posterior Lumbar Interbody Fusion
  • VG1 RAMP - for Posterior Lumbar Interbody Fusion
  • VG1 ALIF - for Anterior Lumbar Body Fusion
FrozenDescriptionSize
VG2TLIF-P9

VG2® TLIF Parallel

Anterior Height = 9 mm
VG2TLIF-P11

VG2® TLIF Parallel

Anterior Height = 11 mm
VG2TLIF-P13

VG2® TLIF Parallel

Anterior Height = 13 mm
VG2TLIF-L9

VG2® TLIF Lordotic

Anterior Height = 9 mm
VG2TLIF-L11

VG2® TLIF Lordotic

Anterior Height = 11 mm
VG2TLIF-L13

VG2® TLIF Lordotic

Anterior Height = 13 mm
68-60-129_vertigraft_shafts.pdf
Description

VertiGRAFT® Fibular Shaft Segments are processed from the fibula, radius or ulna

  • Cortical bone provides biomechanical strength
  • Provided in a variety of sizes to accommodate surgeon's needs and preferences
  • Textured engineering designed for increased surface area and reduced migration
Clinical Application
  • Corpectomy
Freeze-DriedDescriptionSize
VFIBS20

Fibular Textured Shaft

Anterior Height = 20 mm
VFIBS30

Fibular Textured Shaft

Anterior Height = 30 mm
VFIBS40

Fibular Textured Shaft

Anterior Height = 40 mm
VFIBS50

Fibular Textured Shaft

Anterior Height = 50 mm
VFIBS60

Fibular Textured Shaft

Anterior Height = 60 mm
68-60-129.pdf
Description

All Cortical Fibular, Femoral, and Humeral shafts designed to provide biomechanical strength for corpectomy procedures

  • Strength: Cortical Construction
  • Stability: Textured surface area to reduce migration
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1
  • Convenience: Freeze-dried for room temperature storage

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief
Clinical Application
  • Corpectomy Procedures
Freeze-DriedDescriptionSize
VHUMS20

Humeral Shaft

Anterior Height = 20 mm
VHUMS30

Humeral Shaft

Anterior Height = 30 mm
VHUMS40

Humeral Shaft

Anterior Height = 40 mm
VHUMS50

Humeral Shaft

Anterior Height = 50 mm
VHUMS60

Humeral Shaft

Anterior Height = 60 mm
68-60-129.pdf
Description

All Cortical Fibular, Femoral, and Humeral shafts designed to provide biomechanical strength for corpectomy procedures

  • Strength: Cortical Construction 
  • Stability: Textured surface area to reduce migration
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1 
  • Convenience: Freeze-dried for room temperature storage

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief
Clinical Application
  • Corpectomy Procedures
Freeze-DriedDescriptionSize
TIB

Tibial Segment

L = 100 mm
TIB 6.0

Tibial Segment

L = 60 mm
FrozenDescriptionSize
FTSS

Tibial Segment

L = 100mm
FTS

Tibial Segment

L ≥ 200 mm
68-60-129.pdf
Description

All Cortical Fibular, Femoral, and Humeral shafts designed to provide biomechanical strength for corpectomy procedures

  • Strength: Cortical Construction 
  • Stability: Textured surface area to reduce migration
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1 
  • Convenience: Freeze-dried for room temperature storage

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief
Clinical Application
  • Corpectomy Procedures
Freeze-DriedDescriptionSize
FEM

Femoral Shaft

L = 100 mm
FEM 6.0

Femoral Shaft

L = 60 mm
FrozenDescriptionSize
FFS

Femoral Shaft

L ≥ 200 mm
FFSS

Femoral Shaft

L = 100 mm
PreservonDescriptionSize
PFEM 6.0

Femoral Shaft

L = 60 mm
PFEM

Femoral Shaft

L = 100 mm
68-60-129.pdf
Description

All Cortical Fibular, Femoral, and Humeral shafts designed to provide biomechanical strength for corpectomy procedures

  • Strength: Cortical Construction 
  • Stability: Textured surface area to reduce migration
  • Sterile: Sterilized using proprietary and patented Allowash XG® technology. This technology provides a sterility assurance level of 10-6 , without compromising the implant’s inherent osteoconductive properties1 
  • Convenience: Freeze-dried for room temperature storage

 

  1. Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief
Clinical Application
  • Corpectomy Procedures
FrozenDescriptionSize
FHSS

Humeral shaft

L ≥ 200 mm