Other products from "XTANT MEDICAL HOLDINGS, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M697N600016301 N60001630 1/4" BOX CONNECT/JACOBS CHUCK ADAPTER HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT 1 Silex Sacroiliac Joint Fusion System
2 M697N600004721 N60000472 Capless Screw System Ratcheting T-handle HXC WRENCH 1 Silex Sacroiliac Joint Fusion System
3 M697CN6000441 CN60-0044 Specialty Cervical Distractor - Calix HWB EXTRACTOR 1 Calix Spinal Implant System
4 M697C07902661 C079-0266 SPECIAL 12.5mm GRAFT FUNNEL ASSEMBLY HXG Tamp 1 Silex Sacroiliac Joint Fusion System
5 M697C07902651 C079-0265 SPECIAL GRAFT TAMP HXG Tamp 1 Silex Sacroiliac Joint Fusion System
6 M697C07902641 C079-0264 SPECIAL 7mm ADJUSTMENT IMPLANT DRIVER, CANNULATED HXX Screwdriver 1 Silex Sacroiliac Joint Fusion System
7 M697C07902631 C079-0263 Special Guide Handle Assembly, Soft Tissue Shield FZX Guide, Surgical, Instrument 1 Silex Sacroiliac Joint Fusion System
8 M697C07902621 C079-0262 Special Instrument 8mm x 25cm Bone Funnel Assembly HXG Tamp 1 Silex Sacroiliac Joint Fusion System
9 M697C07902611 C079-0261 Special Instrument 8mm x 25cm Tamp Assembly HXG Tamp 1 Silex Sacroiliac Joint Fusion System
10 M697C07900581 C079-0058 Specialty Silex 800 mm Trocar Steinman Pin w/breakaway pt @500mm GDF GUIDE, NEEDLE, SURGICAL Silex Sacroiliac Joint Fusion System
11 M697C07900571 C079-0057 Specialty Silex Aggressive Tip 7mm drill HTW BIT, DRILL 1 Silex Sacroiliac Joint Fusion System
12 M697C07900561 C079-0056 Specialty Silex Aggressive Tip 12.5mm Drill HTW Bit, Drill 1 Silex Sacroiliac Joint Fusion System
13 M697C07900551 C079-0055 Specialty Silex 800 mm Steinmann pin case GDF GUIDE, NEEDLE, SURGICAL 1 Silex Sacroiliac Joint Fusion System
14 M697C07900531 C079-0053 Silex Tissue Spreader Assembly EMF KNIFE, SURGICAL 1 Silex Sacroiliac Joint Fusion System
15 M697C07900521 C079-0052 Specialty Fully Threaded 2.4mm x 300mm Steinmann Pin GDF GUIDE, NEEDLE, SURGICAL 1 Silex Sacroiliac Joint Fusion System
16 M697C07900501 C079-0050 Specialty Jamshidi Awl Insert HWJ AWL 1 Silex Sacroiliac Joint Fusion System
17 M697C07900491 C079-0049 Specialty Cannulated Awl HWJ AWL 1 Silex Sacroiliac Joint Fusion System
18 M697C07900481 C079-0048 Specialty 800mm Long Steinmann Pinn GDF GUIDE, NEEDLE, SURGICAL 1 Silex Sacroiliac Joint Fusion System
19 M697C07900441 C079-0044 Specialty Silex Drill HTW BIT, DRILL 1 Silex Sacroiliac Joint Fusion System
20 M697C07900411 C079-0041 SPECIALTY THREADED STEINMANN PIN 2.4 X 500MM TROCAR TIP GDF GUIDE, NEEDLE, SURGICAL 1 Silex Sacroiliac Joint Fusion System
21 M697C07900391 C079-0039 SPECIALTY #3 STS MORE AGGRESSIVE TIP FZX Guide, surgical, instrument 1 Silex Sacroiliac Joint Fusion System
22 M697C07900381 C079-0038 SPECIALTY #2 STS MORE AGGRESSIVE TIP HWX TAP, BONE 1 Silex Sacroiliac Joint Fusion System
23 M697C07900371 C079-0037 SPECIALTY SILEX WASHER REMOVAL TOOL ASSEMBLY HWB EXTRACTOR 1 Silex Sacroiliac Joint Fusion System
24 M697C07900301 C079-0030 SPECIALTY GUIDE TUBE HANDLE FZX Guide, surgical, instrument 1 Silex Sacroiliac Joint Fusion System
25 M697C07900271 C079-0027 Specialty Silex 12.5mm Tap Aggressive Tip HWX TAP, BONE 1 Silex Sacroiliac Joint Fusion System
26 M697C07900261 C079-0026 CUSTOM IMPACTION DRIVER HWA IMPACTOR 1 Silex Sacroiliac Joint Fusion System
27 M697C07900251 C079-0025 Specialty Silex #3 STS FZX Guide, surgical, instrument 1 Silex Sacroiliac Joint Fusion System
28 M697C07900241 C079-0024 Specialty Silex #2 STS FZX Guide, surgical, instrument 1 Silex Sacroiliac Joint Fusion System
29 M697C07900111 C079-0011 SPECIALTY 12.5 mm IMPLANT DRIVER HXX SCREWDRIVER 1 Silex Sacroiliac Joint Fusion System
30 M697C07900031 C079-0003 SPECIAL 12.5MM TAP HWX TAP, BONE 1 Silex Sacroiliac Joint Fusion System
31 M697C07900021 C079-0002 SPECIAL 12.5MM DRILL HTW BIT, DRILL 1 Silex Sacroiliac Joint Fusion System
32 M697C07900011 C079-0001 CUSTOM #1 SOFT TISSUE SHIELD FZX Guide, surgical, instrument 1 Silex Sacroiliac Joint Fusion System
33 M697C07600061 C076-0006 Specialty Luer Lock adapter for Osteosponge putty syringe MJG DEVICE, PERCUTANEOUS, BIOPSY 1 Zyfix Spinal Facet Screw System
34 M697C07600051 C076-0005 Specialty Luer Lock adapter for Osteosponge putty syringe MJG DEVICE, PERCUTANEOUS, BIOPSY 1 Zyfix Spinal Facet Screw System
35 M697C07600041 C076-0004 Specialty Luer Lock adapter for Osteosponge putty syringe MJG DEVICE, PERCUTANEOUS, BIOPSY 1 Zyfix Spinal Facet Screw System
36 M697X07900341 X079-0034 7mm DRILL BIT, CANNULATED HTW BIT, DRILL 1 Silex Sacroiliac Joint Fusion System
37 00849777011969 C024-0025-PTYV ONE (1) PACKAGE - CONTAINING 2.5cc MBP,MQV Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound 2 CuriGraft DBM Putty, 2.5cc
38 00849777011921 IFLX-CR-05 ONE (1) PACKAGE - CONTAINING 5.0cc MBP,MQV Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound 2 Influx Plus Crunch 5.0cc - Syringe
39 00849777011754 MFC-5 ONE (1) PACKAGE - CONTAINING 5.0cc MBP,MQV Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound 2 MAXX™ Fuse DBM Putty with Chips 5cc
40 00849777011570 X055-0045 10.0cc (Jar) MBP,MQV Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound 2 DMB Putty 10.0cc
41 00849777010535 IS59P025 ONE (1) PACKAGE - CONTAINING 2.5cc MBP,MQV Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound 2 DBM Putty 2.5cc-Syringe
42 00849777010184 BX-600-005-M ONE (1) PACKAGE - CONTAINING 0.5cc MBP,MQV Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound 2 DBM Putty 0.5cc
43 00849777009683 BM895005 ONE (1) PACKAGE - CONTAINING 0.5cc MBP,MQV Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound 2 DBM Putty 0.5cc
44 00849777008778 27800418 ONE (1) PACKAGE - CONTAINING 5.0cc MQV,MBP Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) 2 Reficio DBM Putty 5cc
45 00849777008761 27800218 ONE (1) PACKAGE - CONTAINING 1.0cc MQV,MBP Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) 2 Reficio DBM Putty 1cc
46 00849777008532 DU-25PS ONE (1) PACKAGE - CONTAINING 2.5cc MBP,MQV Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound 2 DBM Putty 2.5cc Syringe
47 00849777008372 X090-0015-PT0.5CCJ ONE (1) PACKAGE - CONTAINING 0.5cc MBP,MQV Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound 2 Axograft DBM Putty 0.5cc - Jar
48 00849777008136 BXS-600-025-M ONE (1) PACKAGE - CONTAINING 2.5cc MQV,MBP Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) 2 DBM Putty 2.5cc in a Syringe
49 00849777007733 NUX-02P ONE (1) PACKAGE - CONTAINING 2.5cc MQV,MBP Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) 2 DBM Putty 2.5cc in a Syringe
50 00849777007474 XT-309025 2.5cc MQV,MBP Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) 2 KBM STERILE PUTTY
Other products with the same Product Codes "MBP, MQV"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00817771028764 Solum IV - 20cc 1201-0200 Solum IV Bone Void Filler CELLING BIOSCIENCES
2 00817771028757 Solum IV - 10cc 1201-0100 Solum IV Bone Void Filler CELLING BIOSCIENCES
3 00817771028740 Solum IV - 5cc 1201-0050 Solum IV Bone Void Filler CELLING BIOSCIENCES
4 00817771028733 Solum IV - 2cc 1201-0020 Solum IV Bone Void Filler CELLING BIOSCIENCES
5 00817771028726 Solum IV - 1cc 1201-0010 Solum IV Bone Void Filler CELLING BIOSCIENCES
6 00817371020632 Solum Flow - 5cc 1206-0050 Solum Flow CELLING BIOSCIENCES
7 00817371020625 Solum Flow - 2cc 1206-0020 Solum Flow CELLING BIOSCIENCES
8 00817337000074 6000041 Tactoset is a synthetic, injectable, settable osteoconductive calcium phosphate Tactoset is a synthetic, injectable, settable osteoconductive calcium phosphate bone graft substitute material. Tactoset ANIKA THERAPEUTICS, INC.
9 00817337000050 6000041 SCS 17-01 is a synthetic, injectable, settable osteoconductive calcium phosphate SCS 17-01 is a synthetic, injectable, settable osteoconductive calcium phosphate bone graft substitute material. SCS 17-01 ANIKA THERAPEUTICS, INC.
10 00816986020518 200X25X8 MM, 40 CC SGFS-040 SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising b SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising biphasic mineral granules and 45S5 bioactive glass suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. SIGNAFUSE Bioactive Bone Graft BIOVENTUS LLC
11 00816986020501 100X25X8 MM, 20 CC SGFS-020 SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising b SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising biphasic mineral granules and 45S5 bioactive glass suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. SIGNAFUSE Bioactive Bone Graft BIOVENTUS LLC
12 00816986020495 50X25X8 MM, 10 CC SGFS-010 SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising b SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising biphasic mineral granules and 45S5 bioactive glass suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. SIGNAFUSE Bioactive Bone Graft BIOVENTUS LLC
13 00816986020488 25X25X8 MM, 5 CC SGFS-005 SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising b SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising biphasic mineral granules and 45S5 bioactive glass suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. SIGNAFUSE Bioactive Bone Graft BIOVENTUS LLC
14 00816986020150 15g MSBG1500 Bioactive Bone Graft Putty UNITE Bioactive Bone Graft BIOVENTUS LLC
15 00816986020143 7.5g MSBG0750 Bioactive Bone Graft Putty UNITE Bioactive Bone Graft BIOVENTUS LLC
16 00816986020136 3.75g MSBG0375 Bioactive Bone Graft Putty UNITE Bioactive Bone Graft BIOVENTUS LLC
17 00816986020129 18cc OMP-18 OSTEOMATRIX+ is a bone graft substitute comprising biphasic mineral granules sus OSTEOMATRIX+ is a bone graft substitute comprising biphasic mineral granules suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. OSTEOMATRIX+ BIOVENTUS LLC
18 00816986020112 9cc OMP-09 OSTEOMATRIX+ is a bone graft substitute comprising biphasic mineral granules sus OSTEOMATRIX+ is a bone graft substitute comprising biphasic mineral granules suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. OSTEOMATRIX+ BIOVENTUS LLC
19 00816986020105 15g OF003 Bioactive Bone Graft Putty OSTEOFUSE BIOVENTUS LLC
20 00816986020099 7.5g OF002 Bioactive Bone Graft Putty OSTEOFUSE BIOVENTUS LLC
21 00816986020082 3.75g OF001 Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixtur Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixture of calcium phosphate granules (CaP) and (45S5) bioactive glass granules suspended in a resorbable alkyleneoxide polymer (AOP) carrier that facilitates handling and delivery of the granule components. The device is supplied as putty, pre-loaded in a syringe applicator and packaged in a sterile barrier foil pouch. The device is provided sterile, for single use, in a variety of sizes. OSTEOFUSE BIOVENTUS LLC
22 00816986020037 IFBG100 IFBG100 INTERFACE is a synthetic bioactive bone graft for use in the repair of osseous d INTERFACE is a synthetic bioactive bone graft for use in the repair of osseous defects. It is supplied as irregular synthetic granules of bioactive glass (45S5 Bioglass), sized from 200 microns to 420 microns. When implanted in living tissue, the material undergoes a time dependent surface modification. The surface reaction results in the formation of a calcium phosphate layer, which is equivalent in composition and structure to the hydroxyapatite found in bone mineral. The biological apatite layer of the granules provides an osteoconductive scaffold for the generation of new osseous tissue. New bone infiltrates around the granules allowing the repair of the defect as the granules are absorbed. INTERFACE BIOVENTUS LLC
23 00816986020020 3.75g SGF-037 Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixtur Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixture of calcium phosphate granules (CaP) and (45S5) bioactive glass granules suspended in a resorbable alkyleneoxide polymer (AOP) carrier that facilitates handling and delivery of the granule components. The device is supplied as putty, pre-loaded in a syringe applicator and packaged in a sterile barrier foil pouch. The device is provided sterile, for single use, in a variety of sizes. SIGNAFUSE BIOVENTUS LLC
24 00816986020013 7.5g SGF-075 Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixtur Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixture of calcium phosphate granules (CaP) and (45S5) bioactive glass granules suspended in a resorbable alkyleneoxide polymer (AOP) carrier that facilitates handling and delivery of the granule components. The device is supplied as putty, pre-loaded in a syringe applicator and packaged in a sterile barrier foil pouch. The device is provided sterile, for single use, in a variety of sizes. SIGNAFUSE BIOVENTUS LLC
25 00816986020006 15g SGF-150 Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixtur Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixture of calcium phosphate granules (CaP) and (45S5) bioactive glass granules suspended in a resorbable alkyleneoxide polymer (AOP) carrier that facilitates handling and delivery of the granule components. The device is supplied as putty, pre-loaded in a syringe applicator and packaged in a sterile barrier foil pouch. The device is provided sterile, for single use, in a variety of sizes. SIGNAFUSE BIOVENTUS LLC
26 00816125022229 RGT-50X25-05 RGT-50X25-05 R-GENIN is a bone void filler consisting of purified bovine collagen, hydroxyapa R-GENIN is a bone void filler consisting of purified bovine collagen, hydroxyapatite, tri-calcium phosphate, and demineralized bone matrix (DBM). The collagen component is biocompatible. After it is implanted, it resorbs and is later replaced by natural bone.R-GENIN 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. The bone graft can be mixed with autogenous blood prior to use at the physician's discretion. R-GENIN Strip BERKELEY ADVANCED BIOMATERIALS, LLC
27 00816125023868 ARM-TCP-BA-12 ARM-TCP-BA-12 HA-TCP-Bioglass Sponge is a bone void filler consisting of a collagen matrix min HA-TCP-Bioglass Sponge is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.HA-TCP-Bioglass Sponge is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. HA-TCP-Bioglass Sponge must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. HA-TCP-Bioglass Sponge BERKELEY ADVANCED BIOMATERIALS, LLC
28 00816125023851 ARM-TCP-10 ARM-TCP-10 HA-TCP Sponge is a sterile bone graft composed of purified fibrillar Type I coll HA-TCP Sponge is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (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.HA-TCP Sponge 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. HA-TCP Sponge BERKELEY ADVANCED BIOMATERIALS, LLC
29 00816125023844 BF-10P BF-10P Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (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.Bi-Ostetic Foam Putty 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. Bi-Ostetic Foam Putty BERKELEY ADVANCED BIOMATERIALS, LLC
30 00816125023837 BF-05P BF-05P Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (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.Bi-Ostetic Foam Putty 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. Bi-Ostetic Foam Putty BERKELEY ADVANCED BIOMATERIALS, LLC
31 00816125023820 BF-02P BF-02P Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (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.Bi-Ostetic Foam Putty 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. Bi-Ostetic Foam Putty BERKELEY ADVANCED BIOMATERIALS, LLC
32 00816125023813 BF-01P BF-01P Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (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.Bi-Ostetic Foam Putty 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. Bi-Ostetic Foam Putty BERKELEY ADVANCED BIOMATERIALS, LLC
33 00816125023806 AA-10P AA-10P Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen m Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.Bi-Ostetic Bioactive Glass Foam is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. Bi-Ostetic Bioactive Glass Foam must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. Bi-Ostetic Bioactive Glass Foam BERKELEY ADVANCED BIOMATERIALS, LLC
34 00816125023790 AA-05P AA-05P Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen m Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.Bi-Ostetic Bioactive Glass Foam is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. Bi-Ostetic Bioactive Glass Foam must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. Bi-Ostetic Bioactive Glass Foam BERKELEY ADVANCED BIOMATERIALS, LLC
35 00816125023783 AA-01P AA-01P Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen m Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.Bi-Ostetic Bioactive Glass Foam is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. Bi-Ostetic Bioactive Glass Foam must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. Bi-Ostetic Bioactive Glass Foam BERKELEY ADVANCED BIOMATERIALS, LLC
36 00816125023776 C10 SWE12 C10 SWE12 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Evans Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
37 00816125023769 C10 SWE10 C10 SWE10 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Evans Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
38 00816125023752 C10 SWE08 C10 SWE08 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Evans Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
39 00816125023745 C10 SWE06 C10 SWE06 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Evans Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
40 00816125023738 C10 SWC08 C10 SWC08 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Cotton Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
41 00816125023721 C10 SWC07 C10 SWC07 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Cotton Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
42 00816125023714 C10 SWC06 C10 SWC06 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Cotton Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
43 00816125023707 C10 SWC05 C10 SWC05 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Cotton Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
44 00816125023691 AMWS-TCP-BA-12 AMWS-TCP-BA-12 HA-TCP-Bioglass Sponge is a bone void filler consisting of a collagen matrix min HA-TCP-Bioglass Sponge is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.HA-TCP-Bioglass Sponge is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. HA-TCP-Bioglass Sponge must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. HA-TCP-Bioglass Sponge BERKELEY ADVANCED BIOMATERIALS, LLC
45 00816125023684 AMWS-TCP-10 AMWS-TCP-10 HA-TCP Sponge is a sterile bone graft composed of purified fibrillar Type I coll HA-TCP Sponge is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (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.HA-TCP Sponge 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. HA-TCP Sponge BERKELEY ADVANCED BIOMATERIALS, LLC
46 00816125023677 OB-10D OB-10D OsteoBoost Select is a bio-engineered mixture of calcium-based inorganic compoun OsteoBoost Select is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, OsteoBoost Select resorbs and is later replaced by natural bone. It provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.OsteoBoost Select is an osteoconductive putty that is 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 putty may be shaped and pressed into the void by hand or inserted into a syringe and injected into the surgical site. The paste set in situ or ex situ provides a void filler that can augment hardware to support bone fragments during the surgical procedure. The set putty acts as a temporary support medium and is not intended to provide structural support during the healing process. The implant is radio-opaque. It is biocompatible and resorbs in the body as bone in-growth occurs. OsteoBoost Select 10cc BERKELEY ADVANCED BIOMATERIALS, LLC
47 00816125023660 OB-05D OB-05D OsteoBoost Select is a bio-engineered mixture of calcium-based inorganic compoun OsteoBoost Select is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, OsteoBoost Select resorbs and is later replaced by natural bone. It provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.OsteoBoost Select is an osteoconductive putty that is 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 putty may be shaped and pressed into the void by hand or inserted into a syringe and injected into the surgical site. The paste set in situ or ex situ provides a void filler that can augment hardware to support bone fragments during the surgical procedure. The set putty acts as a temporary support medium and is not intended to provide structural support during the healing process. The implant is radio-opaque. It is biocompatible and resorbs in the body as bone in-growth occurs. OsteoBoost Select 5cc BERKELEY ADVANCED BIOMATERIALS, LLC
48 00816125023653 M80 SB008 M80 SB008 Tribio™ Implant is a bone void filler consisting of a collagen matrix mineralize Tribio™ Implant is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible. The 45S5 glass particles are bioactive. The device is available in the form of granules, strips, and putty. The composition of the granules is 60 wt% HA and 40 wt% TCP. The amount of 45S5 granules in the graft is 20 wt%. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. This apatite layer on the 45S5 granules and hydroxyapatite-tri-calcium phosphate granules provide an osteoconductive scaffold onto which the patient’s new bone will grow. During healing, the graft particulate is absorbed and remodeled into new bone. Tribio™ Implant, 7.5mm x 40mm BERKELEY ADVANCED BIOMATERIALS, LLC
49 00816125023646 M80 SB006 M80 SB006 Tribio™ Implant is a bone void filler consisting of a collagen matrix mineralize Tribio™ Implant is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible. The 45S5 glass particles are bioactive. The device is available in the form of granules, strips, and putty. The composition of the granules is 60 wt% HA and 40 wt% TCP. The amount of 45S5 granules in the graft is 20 wt%. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. This apatite layer on the 45S5 granules and hydroxyapatite-tri-calcium phosphate granules provide an osteoconductive scaffold onto which the patient’s new bone will grow. During healing, the graft particulate is absorbed and remodeled into new bone. Tribio™ Implant, 5.5mm x 40mm BERKELEY ADVANCED BIOMATERIALS, LLC
50 00816125023639 AA1-100X25-12 AA1-100X25-12 Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen m Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.Bi-Ostetic Bioactive Glass Foam is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. Bi-Ostetic Bioactive Glass Foam must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. Bi-Ostetic Bioactive Glass Foam BERKELEY ADVANCED BIOMATERIALS, LLC