Other products from "RTI SURGICAL, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00191083017198 724-918 724-918 STRMLN TL, LONG HANDLE SCREW INSERTER HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
2 00191083017181 724-874 724-874 STREAMLINE TL STAB AND GRAB FINAL DRIVER HXX SCREWDRIVER 1 Streamline TL Spinal Fixation System
3 00191083017174 724-863 724-863 STRMLN TL, 02-S-FINDER-T,ADD. ETCH LINES LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
4 00191083017167 724-861 724-861 STRMLN TL,NO ROTATE SLEEVE SCRW INSERTER HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
5 00191083017150 724-630 724-630 STREAMLINE TL, FORCEP ROD ROCKER LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
6 00191083017143 724-622 724-622 STRMLN TL 8.5mm HUDSON TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
7 00191083017136 724-621 724-621 STRMLN TL 7.5mm HUDSON TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
8 00191083017129 724-620 724-620 STRMLN TL 6.5mm HUDSON TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
9 00191083017112 724-619 724-619 STRMLN TL 5.5mm HUDSON TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
10 00191083017105 724-618 724-618 STRMLN TL 4.5mm HUDSON TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
11 00191083017099 724-589 724-589 STREAMLINE TL, 3.5mm TAPERED TIP TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
12 00191083017082 724-538 724-538 STRMLN TL FIXED WING TIP INSERTER HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
13 00191083017075 724-444 724-444 STRMLN TL YOKE CAPTURE RS SETSCREW INRTR HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
14 00191083017068 724-440 724-440 STRMLN TL, FIXED HANDLED SCREW INSERTER HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
15 00191083017051 724-439 724-439 STRMLN TL, 7.5mm FIXED HANDLED TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
16 00191083017044 724-438 724-438 STRMLN TL, 6.5mm FIXED HANDLED TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
17 00191083017037 724-437 724-437 STRMLN TL, 5.5mm FIXED HANDLED TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
18 00191083017020 724-436 724-436 STRMLN TL, 4.5mm FIXED HANDLED TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
19 00191083017013 724-387 724-387 STRMLN TL HUDSON CLEANABLE INSERTER HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
20 00191083017006 724-379 724-379 STRMLN TL, 02-C-FINDER-T, PALM HNDL, NC LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
21 00191083016993 724-378 724-378 STRMLN TL, 02-C-FINDER-L, PALM HNDL, NC LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
22 00191083016986 724-377 724-377 STRMLN TL, 02-S-FINDER-T, PALM HNDL, NC LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
23 00191083016979 724-376 724-376 STRMLN TL, 02-S-FINDER-L, PALM HNDL, NC LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
24 00191083016962 724-300 724-300 STRMLN TL STNDRD EASY RELEASE INSERTER HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
25 00191083016955 724-299 724-299 STRMLN TL SHORT EASY RELEASE INSERTER HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
26 00191083016948 724-298 724-298 STREAMLINE TL, 7.0mm TAPERED TIP TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
27 00191083016931 724-252 724-252 STRMLN TL 1/4 SQ SET SCREW INSERTER HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
28 00191083016924 724-246 724-246 STRMLN TL,FIXED T-HANDLE SET SCRW INSRTR HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
29 00191083016917 724-244 724-244 STRMLN TL, CANNULATED SCREW INSERTER HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
30 00191083016900 724-240 724-240 STRMLN TL, 5.5mm CANNULATED 8.5" TAP, UL HWX TAP, BONE 1 Streamline TL Spinal Fixation System
31 00191083016894 724-239 724-239 STRMLN TL, 4.5mm CANNULATED 8.5" TAP, UL HWX TAP, BONE 1 Streamline TL Spinal Fixation System
32 00191083016887 724-211 724-211 STREAMLINE TL SHORT TAP SLEEVE LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
33 00191083016870 724-210 724-210 STREAMLINE TL 8.5mm SHORT TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
34 00191083016863 724-209 724-209 STREAMLINE TL 7.5mm SHORT TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
35 00191083016856 724-208 724-208 STREAMLINE TL 6.5mm SHORT TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
36 00191083016849 724-207 724-207 STREAMLINE TL 5.5mm SHORT TAP HWX TAP, BONE 1 Streamline TL Spinal Fixation System
37 00191083016832 724-206 724-206 STREAMLINE TL 4.5mm SHORT TAP HXW BENDER 1 Streamline TL Spinal Fixation System
38 00191083016825 724-202 724-202 STRMLN TL, REDUCTION SCREW TEE ADJUSTER LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
39 00191083016818 724-200 724-200 STRMLN TL, SCREW ADJUSTER LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
40 00191083016801 724-177 724-177 STRMLN TL, PEDICLE FINDER, HALF FLAT TIP LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
41 00191083016795 724-112 724-112 STRMLN TL, MODULAR REDUCT SCREW INSRTR HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
42 00191083016788 724-008 724-008 STRMLN TL, SCREW INSRTR, NO SPRING SLACK HWR DRIVER, PROSTHESIS 1 Streamline TL Spinal Fixation System
43 00191083016771 724-001 724-001 STRMLN TL 70mm SLIM PED FINDER, STRAIGHT LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
44 00191083016764 723-961 723-961 STRMLN TL, RATCHET TRQ LIMIT T-HANDLE LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Streamline TL Spinal Fixation System
45 00191083016757 10-55-PR-RL-130 10-55-PR-RL-130 ROD, PRE-BENT, R.9.5 KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Streamline TL Spinal Fixation System
46 00191083016740 10-55-PR-RL-125 10-55-PR-RL-125 ROD, PRE-BENT, R.9.5 KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Streamline TL Spinal Fixation System
47 00191083016733 10-55-PR-RL-120 10-55-PR-RL-120 ROD, PRE-BENT, R.9.5 KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Streamline TL Spinal Fixation System
48 00191083016726 10-55-PR-RL-115 10-55-PR-RL-115 ROD, PRE-BENT, R.9.5 KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Streamline TL Spinal Fixation System
49 00191083016719 10-55-PR-RL-110 10-55-PR-RL-110 ROD, PRE-BENT, R.9.5 NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Streamline TL Spinal Fixation System
50 00191083016696 10-55-PR-RL-100 10-55-PR-RL-100 ROD, PRE-BENT, R.9.5 NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Streamline TL Spinal Fixation System
Other products with the same Product Code "MQV"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00868201000188 10 cc Calcium compound bone void filler (10 cc) Fortera VIVORTE, INC
2 00868201000171 5 cc 131133-05-S Calcium compound bone void filler (5 cc) Fortera VIVORTE, INC
3 00868201000164 3 cc 131133-03-S Calcium compound bone void filler (3 cc) Fortera VIVORTE, INC
4 00868201000157 10 cc Calcium compound bone void filler (10 cc) Wizard CaP VIVORTE, INC
5 00868201000140 5 cc Calcium compound bone void filler (5 cc) Wizard CaP VIVORTE, INC
6 00868201000133 3 cc Calcium Bone Void Filler (3 cc) Wizard CaP VIVORTE, INC
7 00868201000126 10 cc 131133-10 Calcium compound bone void filler (10 cc) Trabexus ® VIVORTE, INC
8 00868201000119 5 cc 131133-05 Calcium compound bone void filler (5 cc) Trabexus ® VIVORTE, INC
9 00868201000102 3 cc 131133-03 Calcium compound bone void filler (3cc) Trabexus ® VIVORTE, INC
10 00865179000073 IN012 IQSP-PP-101 1.25cc Paste Mix Plus InQu ISTO TECHNOLOGIES INC
11 00865179000066 IN010 IQSP-PP-102 2.5cc Paste Mix Plus InQu ISTO TECHNOLOGIES INC
12 00865179000059 IN009 IQSP-PP-105 5cc Paste Mix Plus InQu ISTO TECHNOLOGIES INC
13 00865179000042 IN008 IQSP-PP-110 10cc Paste Mix Plus InQu ISTO TECHNOLOGIES INC
14 00865179000035 IN007 IQSP-MX-125 5x5cm Matrix InQu ISTO TECHNOLOGIES INC
15 00865179000028 IN006 IQSP-MX-150 5x10cm Matrix InQu ISTO TECHNOLOGIES INC
16 00865179000011 IN002 IQSP-GR-110 10cc Granules InQu ISTO TECHNOLOGIES INC
17 00865179000004 IN001 IQSP-GR-130 30cc Granules InQu ISTO TECHNOLOGIES INC
18 00863787000478 NGC10X NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. NovoGro Putty OSTEONOVUS, INC.
19 00863787000461 NGC05X NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. NovoGro Putty OSTEONOVUS, INC.
20 00863787000454 NGC025X NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. NovoGro Putty OSTEONOVUS, INC.
21 00863787000430 NGC15 NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. NovoGro Putty OSTEONOVUS, INC.
22 00863787000423 NGC10 NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. NovoGro Putty OSTEONOVUS, INC.
23 00863787000416 NGC05 NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. NovoGro Putty OSTEONOVUS, INC.
24 00863787000409 NGC025 NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. NovoGro Putty OSTEONOVUS, INC.
25 00862835000477 50-003 50-003 Bone Void Filler Kit, 3cc Synthecure AUSTIN MEDICAL VENTURES INC.
26 00862835000453 50-020 50-020 Bone Void Filler Kit, 20cc Synthecure AUSTIN MEDICAL VENTURES INC.
27 00862835000446 50-005 50-005 Bone Void Filler Kit, 5cc Synthecure AUSTIN MEDICAL VENTURES INC.
28 00862835000439 50-010 50-010 Bone Void Filler Kit, 10cc Synthecure AUSTIN MEDICAL VENTURES INC.
29 00862835000422 20-150 20-150 Calcium Sulfate Bone Void Filler, Large Synthecure AUSTIN MEDICAL VENTURES INC.
30 00862835000415 20-125 20-125 Calcium Sulfate Bone Void Filler, Medium Synthecure AUSTIN MEDICAL VENTURES INC.
31 00862835000408 20-112 20-112 Calcium Sulfate Bone Void Filler, Small Synthecure AUSTIN MEDICAL VENTURES INC.
32 00858686006096 100x25x7mm ASI209-20 Bone void filler comprised of 45S5 bioactive glass and a gelatin carrier, intend Bone void filler comprised of 45S5 bioactive glass and a gelatin carrier, intended for implantation NanoFUSE Bioactive Strip AMEND SURGICAL, INC.
33 00858686006089 50x25x7mm ASI209-10 Bone void filler comprised of 45S5 bioactive glass and a gelatin carrier, intend Bone void filler comprised of 45S5 bioactive glass and a gelatin carrier, intended for implantation NanoFUSE Bioactive Strip AMEND SURGICAL, INC.
34 00858686006072 BGP001-10 BGP001-10 Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser Bio V BP Bioactive Glass with DBM Putty AMEND SURGICAL, INC.
35 00858686006065 BGP001-05 BGP001-05 Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser Bio V BP Bioactive Glass with DBM Putty - 5.0 cc AMEND SURGICAL, INC.
36 00858686006058 BGP001-02 BGP001-02 Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser Bio V BP Bioactive Glass with DBM Putty - 2.0 cc AMEND SURGICAL, INC.
37 00858686006041 BGP001-01 BGP001-01 Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser Bio V BP Bioactive Glass with DBM Putty AMEND SURGICAL, INC.
38 00858686006034 NAN109-01 NAN109-01 Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser NanoFuse Bioactive Matrix - 1.0 cc AMEND SURGICAL, INC.
39 00858686006027 NAN109-10 NAN109-10 Synthetic bone void filler containing DBM for orthopedic applications NanoFuse Bioactive Matrix - 10.0 cc AMEND SURGICAL, INC.
40 00858686006010 NAN109-05 NAN109-05 Synthetic bone void filler containing DBM for orthopedic applications NanoFuse Bioactive Matrix - 5.0 cc AMEND SURGICAL, INC.
41 00858686006003 NAN109-02 NAN109-02 Synthetic bone void filler containing DBM for orthopedic applications NanoFuse Bioactive Matrix - 2.0 cc AMEND SURGICAL, INC.
42 00858418003997 BA42-501005 BA42-501005 STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collage STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collagen and 60% hydroxyapatite - 40% tricalcium phosphate resorbable granules. This device, formulated as a block (strip), is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.STRATOFUSE is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30ml. STRATOFUSE Strip BERKELEY ADVANCED BIOMATERIALS, LLC
43 00858418003980 BA41-501005 BA41-501005 STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collage STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collagen and 60% hydroxyapatite - 40% tricalcium phosphate resorbable granules. This device, formulated as a block (strip), is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.STRATOFUSE is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30ml. STRATOFUSE Strip BERKELEY ADVANCED BIOMATERIALS, LLC
44 00858418003973 BA41-501002 BA41-501002 STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collage STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collagen and 60% hydroxyapatite - 40% tricalcium phosphate resorbable granules. This device, formulated as a block (strip), is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.STRATOFUSE is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30ml. STRATOFUSE Strip BERKELEY ADVANCED BIOMATERIALS, LLC
45 00858418003966 SBiO-XYZ400606P SBiO-XYZ400606P SeaSpine Bi-Ostetic Cancellous Blocks is a mixture with a nominal composition of SeaSpine Bi-Ostetic Cancellous Blocks is a mixture with a nominal composition of 60% hydroxyapatite and 40% beta-tri-calcium phosphate. SeaSpine Bi-Ostetic Cancellous Blocks is safe and has excellent biocompatibility. After it is implanted, the implant resorbs and is later replaced by natural bone. SeaSpine Bi-Ostetic Cancellous Blocks is a natural choice for sparing patients the trauma of autograft harvesting. It also provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.SeaSpine Bi-Ostetic Cancellous Blocks is an osteoconductive bone substitute shaped as blocks that are intended to be used to fill voids and gaps that are not intrinsic to the stability of the bone structure. These gaps or voids may be located in the extremities, spine, pelvis, or cranium.The blocks may be pressed into the void or into the surgical site by hand. The SeaSpine Bi-Ostetic Cancellous Blocks provide void filling material that acts as a temporary support medium. The blocks are not intended to provide structural support during the healing process. The implant is radio-opaque. SeaSpine Bi-Ostetic Cancellous Blocks is biocompatible and resorbs in the body as bone ingrowth occurs. SeaSpine Bi-Ostetic Cancellous Block, 40x6x6mm BERKELEY ADVANCED BIOMATERIALS, LLC
46 00858418003959 PCK-10 PCK-10 The Putty Convenience Kit (PCK) is a flexible polymer mat with cavities that all The Putty Convenience Kit (PCK) is a flexible polymer mat with cavities that allows the physician to mold bone putty into beads. Putty Convenience Kit, 10cc BERKELEY ADVANCED BIOMATERIALS, LLC
47 00858418003942 PCK-05 PCK-05 The Putty Convenience Kit (PCK) is a flexible polymer mat with cavities that all The Putty Convenience Kit (PCK) is a flexible polymer mat with cavities that allows the physician to mold bone putty into beads. Putty Convenience Kit, 5cc BERKELEY ADVANCED BIOMATERIALS, LLC
48 00858418003935 EBF1-100X25-15 EBF1-100X25-15 EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 60% hydroxyapatite - 40% tricalcium phosphate resorbable granules. This device is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.EvoGraft is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30 ml. EvoGraft BERKELEY ADVANCED BIOMATERIALS, LLC
49 00858418003928 EBF1-100X25-10 EBF1-100X25-10 EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 60% hydroxyapatite - 40% tricalcium phosphate resorbable granules. This device is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.EvoGraft is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30 ml. EvoGraft BERKELEY ADVANCED BIOMATERIALS, LLC
50 00858418003911 EBF1-90X22-07 EBF1-90X22-07 EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 60% hydroxyapatite - 40% tricalcium phosphate resorbable granules. This device is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.EvoGraft is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30 ml. EvoGraft BERKELEY ADVANCED BIOMATERIALS, LLC