Other products from "PIONEER SURGICAL TECHNOLOGY, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00846468099992 02-95SCREW-CDY 02-95SCREW-CDY SCREW CADDY FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
2 00846468099985 02-CASE-DEF-EMPTY1 02-CASE-DEF-EMPTY1 Instrument Case 1 FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
3 00846468099978 02-CASE-DEF-EMPTY2 02-CASE-DEF-EMPTY2 Instrument Case 2 FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
4 00846468099961 02-FX-AUXCDY-E 02-FX-AUXCDY-E Auxiliary Screw Caddy, Fixed, Empty FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
5 00846468099954 02-LID-RC-LNG 02-LID-RC-LNG Replacement Lid, Long Rod Caddy FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
6 00846468099947 65-C-TRL-M-9-6L 65-C-TRL-M-9-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
7 00846468099930 725-133 725-133 FORTILINK-TS, PISTOL GRIP INSERTER LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Fortilink-TS IBFSystem
8 00846468099848 65-C-TRL-L-11-10L 65-C-TRL-L-11-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
9 00846468099831 65-C-TRL-L-10-10L 65-C-TRL-L-10-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
10 00846468099824 65-C-TRL-L-9-10L 65-C-TRL-L-9-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
11 00846468099817 65-C-TRL-L-8-10L 65-C-TRL-L-8-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
12 00846468099800 65-C-TRL-L-7-10L 65-C-TRL-L-7-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
13 00846468099794 65-C-TRL-L-6-10L 65-C-TRL-L-6-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
14 00846468099787 65-C-TRL-M-11-10L 65-C-TRL-M-11-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
15 00846468099770 65-C-TRL-M-10-10L 65-C-TRL-M-10-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
16 00846468099763 65-C-TRL-M-9-10L 65-C-TRL-M-9-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
17 00846468099756 65-C-TRL-M-8-10L 65-C-TRL-M-8-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
18 00846468099749 65-C-TRL-M-7-10L 65-C-TRL-M-7-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
19 00846468099732 65-C-TRL-M-6-10L 65-C-TRL-M-6-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
20 00846468099725 65-C-TRL-S-11-10L 65-C-TRL-S-11-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
21 00846468099718 65-C-TRL-S-10-10L 65-C-TRL-S-10-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
22 00846468099701 65-C-TRL-S-9-10L 65-C-TRL-S-9-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
23 00846468099695 65-C-TRL-S-8-10L 65-C-TRL-S-8-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
24 00846468099688 65-C-TRL-S-7-10L 65-C-TRL-S-7-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
25 00846468099671 65-C-TRL-S-6-10L 65-C-TRL-S-6-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
26 00846468099602 65-C-TRL-L-11-6L 65-C-TRL-L-11-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
27 00846468099596 65-C-TRL-L-10-6L 65-C-TRL-L-10-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
28 00846468099589 65-C-TRL-L-9-6L 65-C-TRL-L-9-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
29 00846468099572 65-C-TRL-L-8-6L 65-C-TRL-L-8-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
30 00846468099565 65-C-TRL-L-7-6L 65-C-TRL-L-7-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
31 00846468099558 65-C-TRL-L-6-6L 65-C-TRL-L-6-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
32 00846468099541 65-C-TRL-L-5-6L 65-C-TRL-L-5-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
33 00846468099534 65-C-TRL-M-11-6L 65-C-TRL-M-11-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
34 00846468099527 65-C-TRL-M-10-6L 65-C-TRL-M-10-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
35 00846468099510 725-130 725-130 CLARITY II, T-HANDLE DRIVER LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
36 00846468099480 725-128 725-128 CERVALIGN, Ø2.0MM AWL HWJ AWL 1 CervAlign Anterior Cervical Plate System
37 00846468099411 38-PIN-CADDY 38-PIN-CADDY DOCKING PIN CADDY LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
38 00846468099404 38-PIN-90 38-PIN-90 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
39 00846468099398 38-PIN-80 38-PIN-80 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
40 00846468099381 38-PIN-180 38-PIN-180 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
41 00846468099374 38-PIN-170 38-PIN-170 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
42 00846468099367 38-PIN-160 38-PIN-160 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
43 00846468099350 38-PIN-150 38-PIN-150 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
44 00846468099343 38-PIN-140 38-PIN-140 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
45 00846468099336 38-PIN-130 38-PIN-130 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
46 00846468099329 38-PIN-120 38-PIN-120 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
47 00846468099312 38-PIN-110 38-PIN-110 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
48 00846468099305 38-PIN-100 38-PIN-100 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
49 00846468099299 38-LOCKPIN 38-LOCKPIN DILATOR LOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
50 00846468099282 38-180-C-BLD-CADDY 38-180-C-BLD-CADDY 180° CANNULATED BLADE CADDY LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR 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.
39 W4184227005T0473 227005 227005 AFT Diverted Tube (3/4 Filled) DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
40 W4184068100T0473 068100 068100 DBX Putty Inject 10cc DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
41 W4184068050T0473 068050 068050 DBX Putty Inject 5cc DBX® MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.
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