Other products from "ORTHOPEDIATRICS CORP."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00841132184721 00-1300-3173 00-1300-3173 5.5/6.0 Ribbed Pedicle Hook, 11.0mm NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
2 00841132184714 00-1300-3172 00-1300-3172 5.5/6.0 Ribbed Pedicle Hook, 9.5mm KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
3 00841132184707 00-1300-3171 00-1300-3171 5.5/6.0 Ribbed Pedicle Hook, 8.0mm KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
4 00841132184691 00-1300-3170 00-1300-3170 5.5/6.0 Ribbed Pedicle Hook, 6.5mm KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
5 00841132184684 00-1300-3169 00-1300-3169 5.5/6.0 Ribbed Pedicle Hook, 5.0mm NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
6 00841132184653 03-1750-0001 03-1750-0001 NM Case- Tray 1 FSM Tray, Surgical, Instrument 1 Response 5.5/6.0 Spine System
7 00841132184646 03-1800-0002 03-1800-0002 Navigation Instrument Case – Tray 2 FSM TRAY, SURGICAL, INSTRUMENT 1 Response Navigation
8 00841132184639 03-1800-0001 03-1800-0001 Navigation Instrument Case – Tray 1 FSM TRAY, SURGICAL, INSTRUMENT 1 Response Navigation
9 00841132181041 01-1800-2080 01-1800-2080 8.0mm Tap, Cannulated, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
10 00841132181171 01-1800-6038 01-1800-6038 4.5/5.0 Reduction Pedicle Screw Driver, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
11 00841132181034 01-1800-2070 01-1800-2070 7.0mm Tap, Cannulated, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
12 00841132181164 01-1800-6037 01-1800-6037 4.5/5.0 Pedicle Screw Driver, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
13 00841132181157 01-1800-6036 01-1800-6036 5.5/6.0 Reduction Pedicle Screw Driver, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
14 00841132181027 01-1800-2060 01-1800-2060 6.0mm Tap, Cannulated, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
15 00841132181140 01-1800-6035 01-1800-6035 5.5/6.0 Pedicle Screw Driver, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
16 00841132181010 01-1800-2055 01-1800-2055 5.5mm Tap, Cannulated, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
17 00841132181133 01-1800-6022 01-1800-6022 Lenke Probe, Curved, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
18 00841132181126 01-1800-6021 01-1800-6021 Lenke Probe, Straight, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
19 00841132181119 01-1800-3060 01-1800-3060 6.0mm Tap, Single Lead, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
20 00841132181102 01-1800-3055 01-1800-3055 5.5mm Tap, Single Lead, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
21 00841132181096 01-1800-3050 01-1800-3050 5.0mm Tap, Single Lead, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
22 00841132181089 01-1800-3045 01-1800-3045 4.5mm Tap, Single Lead, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
23 00841132181072 01-1800-3040 01-1800-3040 4.0mm Tap, Single Lead, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
24 00841132181065 01-1800-3035 01-1800-3035 3.5mm Tap, Single Lead, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
25 00841132181058 01-1800-3030 01-1800-3030 3.0mm Tap, Single Lead, Navigation OLO Orthopedic stereotaxic instrument 2 Response Navigation
26 00841132180723 XFX-TWST XFX-TWST Tensioner, Wire SB LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 eZ-Fix Tool
27 00841132180693 XFX-625-24L XFX-625-24L Tensioner, Wire LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 eZ-Fix Tool
28 00841132180686 XFX-625-12L XFX-625-12L Statix Hardware LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 eZ-Fix Tool
29 00841132180679 XFX-625 XFX-625 Statix Hardware LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 eZ-Fix Tool
30 00841132178836 01-1300-5155 01-1300-5155 Non-Locking Derotation Handle LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Response Spine System
31 00841132178607 01-9000-3501 01-9000-3501 3.5mm Depth Gauge, Scale Assembly 10-100mm HTJ Gauge, Depth 1 3.5mm Depth Gauge, Scale Assembly 10-100mm
32 00841132178461 03-1750-1000 03-1750-1000 5.5/6.0 Screw Body Extension Caddy FSM TRAY, SURGICAL, INSTRUMENT 1 Response Spine System
33 00841132178447 01-1300-9000 01-1300-9000 Reduction Screw Grasper NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response Spine System
34 00841132177013 00-1300-8200 00-1300-8200 PRE-BENT ROD, Ø5.5MM COCR, 100MM NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
35 00841132177167 00-1300-8300 00-1300-8300 PRE-BENT ROD, Ø6.0MM COCR, 100MM NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
36 00841132177150 00-1300-8395 00-1300-8395 PRE-BENT ROD, Ø6.0MM COCR, 95MM KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
37 00841132177143 00-1300-8390 00-1300-8390 PRE-BENT ROD, Ø6.0MM COCR, 90MM NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
38 00841132177136 00-1300-8385 00-1300-8385 PRE-BENT ROD, Ø6.0MM COCR, 85MM KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
39 00841132177112 00-1300-8375 00-1300-8375 PRE-BENT ROD, Ø6.0MM COCR, 75MM NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
40 00841132177105 00-1300-8370 00-1300-8370 PRE-BENT ROD, Ø6.0MM COCR, 70MM KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
41 00841132177099 00-1300-8365 00-1300-8365 PRE-BENT ROD, Ø6.0MM COCR, 65MM NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
42 00841132177082 00-1300-8360 00-1300-8360 PRE-BENT ROD, Ø6.0MM COCR, 60MM KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
43 00841132177075 00-1300-8355 00-1300-8355 PRE-BENT ROD, Ø6.0MM COCR 55MM NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
44 00841132177068 00-1300-8350 00-1300-8350 PRE-BENT ROD, Ø6.0MM COCR, 50MM KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
45 00841132177051 00-1300-8345 00-1300-8345 PRE-BENT ROD, Ø6.0MM COCR, 45MM NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
46 00841132177044 00-1300-8340 00-1300-8340 PRE-BENT ROD, Ø6.0MM COCR, 40MM KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
47 00841132177037 00-1300-8335 00-1300-8335 PRE-BENT ROD, Ø6.0MM COCR, 35MM KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
48 00841132177020 00-1300-8330 00-1300-8330 PRE-BENT ROD, Ø6.0MM COCR, 30MM KWP,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Thoracolumbosacral pedicle screw system 2 Response 5.5/6.0 Spine System
49 00841132177006 00-1300-8295 00-1300-8295 PRE-BENT ROD, Ø5.5MM COCR, 95MM NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
50 00841132176993 00-1300-8290 00-1300-8290 PRE-BENT ROD, Ø5.5MM COCR, 90MM NKB,KWP Thoracolumbosacral pedicle screw system,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Response 5.5/6.0 Spine System
Other products with the same Product Code "MQV"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 50601557114230 Genex® Bone Graft Substitute 10cc 910-010 Genex® Bone Graft Substitute is a simple to use synthetic resorbable material de Genex® Bone Graft Substitute is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form Genex® Bone Graft Substitute a hard but resorbable matrix. Genex® Bone Graft Substitute is supplied sterile. Genex® BIOCOMPOSITES LTD
2 50601557114162 Genex® Bone Graft Substitute 5cc 910-005 Genex® Bone Graft Substitute is a simple to use synthetic resorbable material de Genex® Bone Graft Substitute is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form Genex® Bone Graft Substiute, a hard but resorbable matrix. Genex® Bone Graft Substitute is supplied sterile. Genex® BIOCOMPOSITES LTD
3 50601557110966 11-2002 11-2002 geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. One component of the matrix prevents soft tissue in-growth until it is resorbed and replaced by new bony tissue. Another component has been shown to act as a scaffold through which new bone grows. The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form geneX®; a hard but resorbable matrix. geneX® ds BIOCOMPOSITES LTD
4 50601557110898 11-2005 11-2005 geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. One component of the matrix prevents soft tissue in-growth until it is resorbed and replaced by new bony tissue. Another component has been shown to act as a scaffold through which new bone grows. The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form geneX®; a hard but resorbable matrix. geneX® ds BIOCOMPOSITES LTD
5 50601557110584 640-005 640-005 Stimulan® DS Calcium Sulfate Bone Void Filler is provided sterile for single pat Stimulan® DS Calcium Sulfate Bone Void Filler is provided sterile for single patient use. The kit contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together, the resultant paste is to be injected or digitally packed into open bone/gap to cure insitu. The biodegradable, radiopaque mixture is resorbed in approximately 30-60 days when used in accordance with the device labelling. Stimulan® is manufactured from synthetic implant grade calcium sulfate dihydrate (CaS04, 2H20) that resporbs and is replaced with bone during the healing process. Also as the bone void filler is biodegradable and biocompatible; it may be used at an infected site. Stimulan® DS BIOCOMPOSITES LTD
6 50601557110416 620-020 620-020 STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. Stimulan® Rapid Cure BIOCOMPOSITES LTD
7 50601557110348 620-010 620-010 STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. Stimulan® Rapid Cure BIOCOMPOSITES LTD
8 50601557110270 620-005 620-005 STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. Stimulan® Rapid Cure BIOCOMPOSITES LTD
9 50601557109694 980-005 980-005 geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. One component of the matrix prevents soft tissue in-growth until it is resorbed and replaced by new bony tissue. Another component has been shown to act as a scaffold through which new bone grows. The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe.When injected the mixture sets to form geneX®; a hard but resorbable matrix. geneX® ds BIOCOMPOSITES LTD
10 50601557109526 980-002 980-002 geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. One component of the matrix prevents soft tissue in-growth until it is resorbed and replaced by new bony tissue. Another component has been shown to act as a scaffold through which new bone grows. The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe.When injected the mixture sets to form geneX®; a hard but resorbable matrix. geneX® ds BIOCOMPOSITES LTD
11 50601557101810 920-010 920-010 geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Pu geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Putty has been bioengineered to mimic human bone. It is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. geneX® Putty is a non-setting putty and is supplied sterile. geneX® putty BIOCOMPOSITES LTD
12 50601557101742 920-005 920-005 geneX® putty consists of an inorganic framework of calcium based ions. geneX® Pu geneX® putty consists of an inorganic framework of calcium based ions. geneX® Putty has been bioengineered to mimic human bone. It is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. geneX® Putty is a non-setting putty and is supplied sterile. geneX® Putty BIOCOMPOSITES LTD
13 50601557101674 920-002 920-002 geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Pu geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Putty has been bioengineered to mimic human bone. It is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. geneX® Putty is a non-setting putty and is supplied sterile. geneX® putty BIOCOMPOSITES LTD
14 50601557101506 900-010 900-010 geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form geneX® a hard but resorbable matrix. geneX® is supplied sterile geneX® BIOCOMPOSITES LTD
15 50601557101438 900-005 900-005 geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form geneX® a hard but resorbable matrix. geneX® is supplied sterile geneX® BIOCOMPOSITES LTD
16 50601557101292 600-010 600-010 STIMULAN® Kit - provided sterile for single patient use. STIMULAN® Kit contains STIMULAN® Kit - provided sterile for single patient use. STIMULAN® Kit contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be injected or digitally packed into open bone void/gap to set in situ or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Kit is manufactured from synthetic implant grade calcium sulfate dihydrate (CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. Stimulan® Kit BIOCOMPOSITES LTD
17 50601557101124 600-005 600-005 STIMULAN® Kit - provided sterile for single patient use. STIMULAN® Kit contains STIMULAN® Kit - provided sterile for single patient use. STIMULAN® Kit contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be injected or digitally packed into open bone void/gap to set in situ or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Kit is manufactured from synthetic implant grade calcium sulfate dihydrate (CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. Stimulan® Kit BIOCOMPOSITES LTD
18 50601557100998 600-30-s1 600-30-s1 Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for sing Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for single patient use. The biodegradable, radiopaque pellets are resorbed in approximately 30-60 days when used in accordance with the device labelling. Calcium Sulfate Bone Filler is manufactured from medical grade calcium sulfate dihydrate (CaSO4 2H20) and stearic acid that resorbs and is replaced with bone during the healing process. Also as the bone void filler pellets are biodegradable and biocompatible, they may be used at an infected site. Stimulan® Dispenser BIOCOMPOSITES LTD
19 50601557100752 600-48-010 600-48-010 Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for sing Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for single patient use. The biodegradable, radiopaque pellets are resorbed in approximately 30-60 days when used in accordance with the device labelling. Calcium Sulfate Bone Filler is manufactured from medical grade calcium sulfate dihydrate (CaSO4 2H20) and stearic acid that resorbs and is replaced with bone during the healing process. Also as the bone void filler pellets are biodegradable and biocompatible, they may be used at an infected site. Stimulan® Pellets BIOCOMPOSITES LTD
20 50601557100516 600-30-005 600-30-005 Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for sing Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for single patient use. The biodegradable, radiopaque pellets are resorbed in approximately 30-60 days when used in accordance with the device labelling. Calcium Sulfate Bone Filler is manufactured from medical grade calcium sulfate dihydrate (CaSO4 2H20) and stearic acid that resorbs and is replaced with bone during the healing process. Also as the bone void filler pellets are biodegradable and biocompatible, they may be used at an infected site. Stimulan® Pellets BIOCOMPOSITES LTD
21 50601557100448 800-020 800-020 Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for single patient use. The biodegradable, radiopaque granules/blocks are resorbed in approximately 6-12 months when used in accordance with the device labelling. Biocomposites Tri-Calcium Phosphate Bone Graft Substitute is manufactured from medical grade Tri-Calcium Phosphate. Numerous bone graft operations are undertaken every year to repair bone defects caused by surgery, tumours, trauma, infections and other damage. Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is intended for use in clinical situations where the use of autologous grafts or other bone graft substitutes maybe undesirable, due either to the risk of associated infection or unavailability. Allogran-R® resorbs and is replaced with bone during the healing process. Allogran-R® BIOCOMPOSITES LTD
22 50601557100370 800-010 800-010 Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for single patient use. The biodegradable, radiopaque granules/blocks are resorbed in approximately 6-12 months when used in accordance with the device labelling. Biocomposites Tri-Calcium Phosphate Bone Graft Substitute is manufactured from medical grade Tri-Calcium Phosphate. Numerous bone graft operations are undertaken every year to repair bone defects caused by surgery, tumours, trauma, infections and other damage. Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is intended for use in clinical situations where the use of autologous grafts or other bone graft substitutes maybe undesirable, due either to the risk of associated infection or unavailability. Allogran-R® resorbs and is replaced with bone during the healing process. Allogran-R® BIOCOMPOSITES LTD
23 50601557100202 800-005 800-005 Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for single patient use. The biodegradable, radiopaque granules/blocks are resorbed in approximately 6-12 months when used in accordance with the device labelling. Biocomposites Tri-Calcium Phosphate Bone Graft Substitute is manufactured from medical grade Tri-Calcium Phosphate. Numerous bone graft operations are undertaken every year to repair bone defects caused by surgery, tumours, trauma, infections and other damage. Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is intended for use in clinical situations where the use of autologous grafts or other bone graft substitutes maybe undesirable, due either to the risk of associated infection or unavailability. Allogran-R® resorbs and is replaced with bone during the healing process. Allogran-R® BIOCOMPOSITES LTD
24 W4184428025T0473 428025 428025 DBX Putty 2.5cc DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
25 W4184428010T0473 428010 428010 DBX Putty 1cc DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
26 W4184428005T0473 428005 428005 DBX Putty 0.5cc DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
27 W4184420810T0473 420810 420810 Legacy DBM, 10CC Legacy DBM MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
28 W4184420805T0473 420805 420805 Legacy DBM, 5CC Legacy DBM MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
29 W4184420802T0473 420802 420802 Legacy DBM, 2.5CC Legacy DBM MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
30 W4184420801T0473 420801 420801 Legacy DBM, 1CC Legacy DBM MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
31 W4184420800T0473 420800 420800 Legacy DBM, 0.5cc Legacy DBM MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
32 W4184228025T0473 228025 228025 DBX Putty 2.5cc DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
33 W4184228010T0473 228010 228010 DBX Putty 1cc DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
34 W4184228005T0473 228005 228005 DBX Putty 0.5cc DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
35 W4184227060T0473 227060 227060 AFT-DS Straight Tube (7/8-filled) DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
36 W4184227055T0473 227055 227055 AFT-DS Diverted Tube (7/8-filled) DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
37 W4184227010T0473 227010 227010 AFT Straight Tube (1/2 Filled) DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
38 W4184227007T0473 227007 227007 AFT Straight Tube (3/4 Filled) DBX MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
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