Other products from "SYNTHES GMBH"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 10886982181770 294.767 294767 4.0MM/2.5MM SCHANZ SCREW 18MM THRD/65MM LXT,KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COM APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT 2 NA
2 10886982195944 357.25 35725 SLIDE HAMMER FOR HAMMER GUIDE FZY HAMMER, SURGICAL 1 NA
3 10886982195920 357.221 357221 FEMORAL NAIL HAMMER GUIDE LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT NA
4 10886982195913 357.22 35722 HAMMER GUIDE FOR SLIDE HAMMER FZY HAMMER, SURGICAL NA
5 10886982195906 357.181 357181 FEMORAL NAIL DRIVING ADAPTOR LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT NA
6 10886982195883 357.133 357133 EXTRACTION SCREW FOR TI FEMORAL AND TIBIAL NAILS HWB EXTRACTOR 1 NA
7 10886982195876 357.128 357128 13.0MM/3.2MM TROCAR FZX Guide, surgical, instrument 1 NA
8 10886982195357 356.309 356309 9MM TREPHINE HWK TREPHINE 1 NA
9 10886982195869 357.127 357127 13.0MM PROTECTION SLEEVE FZX Guide, surgical, instrument 1 NA
10 10886982195791 357.096 357096 AIMING ARM FOR 6.0MM TI LOCKING SCREWS FZX Guide, surgical, instrument NA
11 10886982195784 357.095 357095 CONNECTING SCREW FOR TI DISTAL FEMORAL NAILS LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
12 10886982195777 357.073 357073 EXTRACTION HOLDING SLEEVE FOR HIP PIN FZX Guide, surgical, instrument 1 NA
13 10886982195753 357.055 357055 SCREWDRIVER HEXAGONAL CANNULATED L365MM HXX SCREWDRIVER 1 NA
14 10886982195746 357.054 357054 T-HANDLE HXC WRENCH 1 NA
15 10886982195739 357.052 357052 TROCHANTERIC FIXATION NAIL SCREW COMPRESSION NUT HWC,HSB Screw, fixation, bone,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES NA
16 10886982195722 357.051 357051 COUPLING SCREW HXC WRENCH 1 NA
17 10886982195715 357.047 357047 6.5MM CANNULATED DRILL BIT QC/330MM HTW BIT, DRILL 1 NA
18 10886982195708 357.046 357046 FIXATION SLEEVE HTW,FZX BIT, DRILL,Guide, surgical, instrument 1 NA
19 10886982195692 357.039 357039 2.8MM GUIDE WIRE 350MM JDW,JDS PIN, FIXATION, THREADED,NAIL, FIXATION, BONE 2 NA
20 10886982195685 356.982 356982 4.0MM THREE-FLUTED DRILL BIT QC/215MM/80MM CALIB GFF,HSZ,HWE,GFA BUR, SURGICAL, GENERAL & PLASTIC SURGERY,Instrument, surgical, orthopedic, pneum BUR, SURGICAL, GENERAL & PLASTIC SURGERY,Instrument, surgical, orthopedic, pneumatic powered & accessory/attachment,INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT,BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL 1 NA
21 10886982195678 356.98 35698 4.0MM THREE-FLUTED DRILL BIT QC/270MM/95MM CALIB GFF,HWE,GFA,HSZ BUR, SURGICAL, GENERAL & PLASTIC SURGERY,INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-PO BUR, SURGICAL, GENERAL & PLASTIC SURGERY,INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT,BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL,Instrument, surgical, orthopedic, pneumatic powered & accessory/attachment 1 NA
22 10886982195654 356.972 356972 3.2MM THREE-FLUTED DRILL BIT QC/215MM/82MM CALIBRATION HTW BIT, DRILL 1 NA
23 10886982195647 356.97 35697 3.2MM THREE-FLUTED DRILL BIT QC/215MM/80MM CALIB HTW BIT, DRILL 1 NA
24 10886982195623 356.830 356830 GUIDE WIRE 3.2MM FOR PFNA BLADE FZX Guide, surgical, instrument 1 NA
25 10886982195616 356.825 356825 EXTRACTION SCREW FOR PFNA BLADE HWB EXTRACTOR 1 NA
26 10886982195609 356.717 356717 GUIDE WIRE 2.8MM LENGTH 460MM WITH HOOK HWB EXTRACTOR 1 NA
27 10886982195517 356.544 356544 INSERTION BOLT FOR TI CANNULATED TIBIAL NAIL FZX Guide, surgical, instrument 1 NA
28 10886982195500 356.543 356543 EXTRACTION SCREW FOR TITANIUM TIBIAL NAIL LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
29 10886982195494 356.542 356542 INSERTION BOLT FOR SOLID TIBIAL NAIL FZX Guide, surgical, instrument 1 NA
30 10886982195463 356.49 35649 INSERTER-EXTRACTOR FOR TI TIBIAL & HUMERAL NAILS HWB EXTRACTOR 1 NA
31 10886982195456 356.350 356350 RATCHET GRIP HWB EXTRACTOR 1 NA
32 10886982195449 356.340 356340 DRIVE SHAFT 490MM HWB EXTRACTOR 1 NA
33 10886982195432 356.332 356332 EXTRACTOR HEAD F/12MM NAILS HWB EXTRACTOR 1 NA
34 10886982195425 356.331 356331 EXTRACTOR HEAD F/11MM NAILS HWB EXTRACTOR 1 NA
35 10886982195418 356.330 356330 EXTRACTOR HEAD F/10MM NAILS HWB EXTRACTOR 1 NA
36 10886982195401 356.329 356329 EXTRACTOR HEAD F/9MM NAILS HWB EXTRACTOR 1 NA
37 10886982195395 356.328 356328 EXTRACTOR HEAD F/8MM NAILS HWB EXTRACTOR 1 NA
38 10886982195388 356.312 356312 12MM TREPHINE HWK TREPHINE 1 NA
39 10886982195371 356.311 356311 11MM TREPHINE HWK TREPHINE 1 NA
40 10886982195364 356.310 356310 10MM TREPHINE HWK TREPHINE 1 NA
41 10886982195234 355.89 35589 6.0MM/5.0MM DRILL SLEEVE FZX Guide, surgical, instrument 1 NA
42 10886982195227 355.88 35588 5.0MM/3.5MM DRILL SLEEVE FZX Guide, surgical, instrument 1 NA
43 10886982195210 355.87 35587 3.5MM TROCAR FZX Guide, surgical, instrument 1 NA
44 10886982195203 355.75 35575 8.0MM TROCAR FZX Guide, surgical, instrument 1 NA
45 10886982195081 355.59 35559 LOCKING NUT FOR 17MM-19MM UNIVERSAL FEMORAL NAILS LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
46 10886982195074 355.58 35558 LOCKING NUT FOR 13MM-16MM UNIVERSAL FEMORAL NAILS LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
47 10886982195067 355.57 35557 LOCKING NUT FOR 9MM-12MM UNIVERSAL FEMORAL NAILS LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
48 10886982195050 355.55 35555 THREADED CONICAL BOLT FOR 17MM-19MM UNIV FEMORAL NAILS LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
49 10886982195043 355.54 35554 THREADED CONICAL BOLT FOR 13MM-16MM UNIV FEMORAL NAILS LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
50 10886982195036 355.53 35553 THREADED CONICAL BOLT FOR 9MM-12MM UNIV FEMORAL NAILS LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
Other products with the same Product Code "MQV"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00817371020632 Solum Flow - 5cc 1206-0050 Solum Flow CELLING BIOSCIENCES
2 00817371020625 Solum Flow - 2cc 1206-0020 Solum Flow CELLING BIOSCIENCES
3 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.
4 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.
5 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
6 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
7 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
8 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
9 00816986020150 15g MSBG1500 Bioactive Bone Graft Putty UNITE Bioactive Bone Graft BIOVENTUS LLC
10 00816986020143 7.5g MSBG0750 Bioactive Bone Graft Putty UNITE Bioactive Bone Graft BIOVENTUS LLC
11 00816986020136 3.75g MSBG0375 Bioactive Bone Graft Putty UNITE Bioactive Bone Graft BIOVENTUS LLC
12 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
13 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
14 00816986020105 15g OF003 Bioactive Bone Graft Putty OSTEOFUSE BIOVENTUS LLC
15 00816986020099 7.5g OF002 Bioactive Bone Graft Putty OSTEOFUSE BIOVENTUS LLC
16 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
17 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
18 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
19 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
20 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
21 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
22 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
23 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
24 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
25 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
26 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
27 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
28 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
29 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
30 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
31 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
32 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
33 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
34 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
35 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
36 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
37 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
38 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
39 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
40 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
41 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
42 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
43 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
44 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
45 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
46 00816125023622 AA1-50X25-06 AA1-50X25-06 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
47 00816125023615 7888-0125 7888-0125 OptiFuse BA is a bone void filler consisting of a collagen matrix mineralized wi OptiFuse BA 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.OptiFuse BA 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. OptiFuse BA must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. OptiFuse BA 12.5cc Strip BERKELEY ADVANCED BIOMATERIALS, LLC
48 00816125023608 7888-0063 7888-0063 OptiFuse BA is a bone void filler consisting of a collagen matrix mineralized wi OptiFuse BA 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.OptiFuse BA 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. OptiFuse BA must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. OptiFuse BA 6.25cc Strip BERKELEY ADVANCED BIOMATERIALS, LLC
49 00816125023592 BF1-100X25-05 BF1-100X25-05 Bi-Ostetic Foam Strip is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Strip 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 Strip 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 Strip BERKELEY ADVANCED BIOMATERIALS, LLC
50 00816125023585 BF1-50X25-02 BF1-50X25-02 Bi-Ostetic Foam Strip is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Strip 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 Strip 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 Strip BERKELEY ADVANCED BIOMATERIALS, LLC