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.

fibular_wedge_68-60-037-01_.00_.pdf

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

Clinical Application

Anterior Cervical Fusion
Trauma

Fibular Segment, VertiGraft® Fibula/Radius/Ulna Wedge

Frozen	Description	Size
FFIBW8	Fibula/Radius/Ulna Wedge	H = 18 mm

Freeze-Dried	Description	Size
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-Dried	Description	Size
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

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

Preservon	Description	Size
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

Abla, Adnan, et al. (2005) Allograft Composite Cortical and Cancellous Bone Graft for Anterior Cervical Fusion. Contemporary Neurosurgery. 27(8).
Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG®.” 2007 Bio-Implants Brief.
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

Preservon	Description	Size
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

Frozen	Description	Size
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

68-60-040-01.pdf

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

Clinical Application

Anterior Cervical and Lumbar Fusion

Freeze-Dried	Description	Size
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)

Preservon	Description	Size
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

68-65-014_matrigraft_tricort.pdf

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

Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers.
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-Dried	Description	Size
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

Preservon	Description	Size
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

68-65-063_matrigraft_uni_spacer.pdf

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

Clinical Application

Anterior Cervical Fusion

Tricortical Cancellous Wedge-Parallel, Iliac Crest Wedge

Measurements

L = 11 mm and W = 14 mm

Freeze-Dried	Description	Size
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

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

Preservon	Description	Size
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

Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data of file at LifeNet Health.
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

Preservon	Description	Size
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-Dried	Description	Size
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

68-65-093_acis_vg2.pdf

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

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)

Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data of file at LifeNet Health.
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-Dried	Description	Size
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

Preservon	Description	Size
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-Dried	Description	Size
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 potential^1-4
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)

Zhang M, Powers R, Wolfinbarger L. (1997). Effect(s) of demineralization process on the osteoinductivity of demineralized bone matrix. J Periodontol, 68:1085-1092.
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.
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.
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.
Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG^®.” 2007 Bio-Implants Brief.

Clinical Application

Any surgical application that requires bone void filler

Freeze-Dried	Description	Size
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 potential^1-4
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)

Zhang M, Powers R, Wolfinbarger L. (1997). Effect(s) of demineralization process on the osteoinductivity of demineralized bone matrix. J Periodontol, 68:1085-1092.
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.
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.
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.
Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG^®.” 2007 Bio-Implants Brief.

Clinical Application

Any surgical application that requires bone void filler

Freeze-Dried	Description	Size
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-Dried	Description	Size
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-Dried	Description	Size
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

68-65-020_optium.pdf

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
Everly 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

Clinical Application

Joint Reconstruction and Revision
Trauma
Spine

I/C Graft Chamber® and Optium® DBM Gel

Freeze-Dried	Description	Size
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

68-65-020_optium.pdf

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

Clinical Application

Joint Reconstruction and Revision
Trauma
Spine

Freeze-Dried	Description	Size
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 potential^1-4
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)

Zhang M, Powers R, Wolfinbarger L. (1997). Effect(s) of demineralization process on the osteoinductivity of demineralized bone matrix. J Periodontol, 68:1085-1092.
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.
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.
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.
Eisenlohr LM. “Allograft Tissue Sterilization Using Allowash XG^®.” 2007 Bio-Implants Brief.

Clinical Application

Any surgical application that requires bone void filler

Freeze-Dried	Description	Size
DCC1/4	Demineralized Cortical/Cancellous	20 cc

68-60-027-02_readigraft.pdf

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.

Clinical Application

Any surgical application that requires bone void filler

Freeze-Dried	Description	Size
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)

Independent sources include the Virginia Commonwealth University Medical Center and the American Association of Mechanical Engineers. Data of file at LifeNet Health.
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-Dried	Description	Size
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

Frozen	Description	Size
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

Preservon	Description	Size
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

68-60-141.pdf

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

PliaFX Video

• Osteoinductive Potential: Optimally demineralized by LifeNet Health’s patented and proprietary PAD^® technology to expose natural growth factors^1-5

• 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

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 Temperature	Description	Size
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

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

Frozen	Description	Size
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-Dried	Description	Size
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

Preservon	Description	Size
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

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

Clinical Application

Spinal fusion inter-body and discectomy procedures

Freeze-Dried	Description	Size
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

vertigraft_vg2_plif_68-65-027.pdf

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

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

Frozen	Description	Size
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

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

Frozen	Description	Size
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

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

Frozen	Description	Size
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-Dried	Description	Size
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

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

Clinical Application

Corpectomy Procedures

Freeze-Dried	Description	Size
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

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

Clinical Application

Corpectomy Procedures

Freeze-Dried	Description	Size
TIB	Tibial Segment	L = 100 mm
TIB 6.0	Tibial Segment	L = 60 mm

Frozen	Description	Size
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

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

Clinical Application

Corpectomy Procedures

Freeze-Dried	Description	Size
FEM	Femoral Shaft	L = 100 mm
FEM 6.0	Femoral Shaft	L = 60 mm

Frozen	Description	Size
FFS	Femoral Shaft	L ≥ 200 mm
FFSS	Femoral Shaft	L = 100 mm

Preservon	Description	Size
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

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

Clinical Application

Corpectomy Procedures

Frozen	Description	Size
FHSS	Humeral shaft	L ≥ 200 mm

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