Other products from "NUVASIVE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00887517399779 6942044 CoRoent® XLR, 20x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
2 00887517399700 6941844 CoRoent® XLR, 18x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
3 00887517399335 6941644 CoRoent® XLR, 16x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
4 00887517398765 6941444 CoRoent® XLR, 14x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
5 00887517398499 6941244 CoRoent® XLR, 12x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
6 00887517398420 6941044 CoRoent® XLR, 10x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
7 00887517398055 6932088 CoRoent® XLR, 20x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
8 00887517397683 6931888 CoRoent® XLR, 18x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
9 00887517397256 6931688 CoRoent® XLR, 16x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
10 00887517396822 6931488 CoRoent® XLR, 14x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
11 00887517396457 6931288 CoRoent® XLR, 12x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
12 00887517395641 6922088 CoRoent® XLR, 20x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
13 00887517395634 6922044 CoRoent® XLR, 20x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
14 00887517395269 6921888 CoRoent® XLR, 18x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
15 00887517395252 6921844 CoRoent® XLR, 18x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
16 00887517394880 6921688 CoRoent® XLR, 16x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
17 00887517394873 6921660 CoRoent® XL Wide, 16x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
18 00887517394866 6921655 CoRoent® XL Wide, 16x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
19 00887517394859 6921650 CoRoent® XL Wide, 16x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
20 00887517394842 6921645 CoRoent® XL Wide, 16x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
21 00887517394835 6921644 CoRoent® XLR, 16x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
22 00887517394569 6921488 CoRoent® XLR, 14x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
23 00887517394552 6921460 CoRoent® XL Wide, 14x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
24 00887517394545 6921455 CoRoent® XL Wide, 14x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
25 00887517394538 6921450 CoRoent® XL Wide, 14x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
26 00887517394521 6921445 CoRoent® XL Wide, 14x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
27 00887517394514 6921444 CoRoent® XLR, 14x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
28 00887517394149 6921288 CoRoent® XLR, 12x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
29 00887517394132 6921260 CoRoent® XL Wide, 12x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
30 00887517394125 6921255 CoRoent® XL Wide, 12x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
31 00887517394118 6921250 CoRoent® XL Wide, 12x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
32 00887517394101 6921245 CoRoent® XL Wide, 12x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
33 00887517393791 6921244 CoRoent® XLR, 12x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
34 00887517393722 6921088 CoRoent® XLR, 10x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
35 00887517393715 6921060 CoRoent® XL Wide, 10x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
36 00887517393708 6921055 CoRoent® XL Wide, 10x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
37 00887517393395 6921050 CoRoent® XL Wide, 10x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
38 00887517393388 6921045 CoRoent® XL Wide, 10x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
39 00887517393371 6921044 CoRoent® XLR, 10x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
40 00887517393333 6920860 CoRoent® XL Wide, 8x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
41 00887517393326 6920855 CoRoent® XL Wide, 8x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
42 00887517393319 6920850 CoRoent® XL Wide, 8x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
43 00887517393302 6920845 CoRoent® XL Wide, 8x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
44 00887517392961 6916860 CoRoent® XL, 16x18x60mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
45 00887517392954 6916855 CoRoent® XL, 16x18x55mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
46 00887517392947 6916850 CoRoent® XL, 16x18x50mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
47 00887517392930 6916845 CoRoent® XL, 16x18x45mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
48 00887517392923 6916840 CoRoent® XL, 16x18x40mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
49 00887517392916 6916260 CoRoent® XL Wide, 16x22x60mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
50 00887517392909 6916255 CoRoent® XL Wide, 16x22x55mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
Other products with the same Product Codes "MBP, MQV"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M958BSF251000 BSF-25100 BioSphere Flex, Large BioSphere Flex, Large SYNERGY BIOMEDICAL, LLC
2 M958BSF250500 BSF-25050 BioSphere Flex, Medium BioSphere Flex, Medium SYNERGY BIOMEDICAL, LLC
3 M958BSF00150 Large BSF-00150 BioSphere Flex SP SYNERGY BIOMEDICAL, LLC
4 M958BSF00075 Medium BSF-00075 BioSphere Flex SP SYNERGY BIOMEDICAL, LLC
5 M958BSF000400 BSF-00040 BioSphere Flex SP Extremities, Medium BioSphere Flex SP Extremities, Medium SYNERGY BIOMEDICAL, LLC
6 M958BSF000300 BSF-00030 BioSphere Flex SP Extremities, Small BioSphere Flex SP Extremities, Small SYNERGY BIOMEDICAL, LLC
7 M958BPY1000R 10cc BPY-100 BioSphere Putty SYNERGY BIOMEDICAL, LLC
8 M958BPY1000 10cc BPY-100 BioSphere Putty SYNERGY BIOMEDICAL, LLC
9 M958BPY0500V 5cc BPY-050 BioSphere Putty SYNERGY BIOMEDICAL, LLC
10 M958BPY0500 5cc BPY-050 BioSphere Putty SYNERGY BIOMEDICAL, LLC
11 M958BPY0250X 2.5cc BPY-025 BioSphere Putty SYNERGY BIOMEDICAL, LLC
12 M958BPY0250 2.5cc BPY-025 BioSphere Putty SYNERGY BIOMEDICAL, LLC
13 M958BPY0010R 1cc BPY-001 BioSphere Putty SYNERGY BIOMEDICAL, LLC
14 M958BPY0010 1cc BPY-001 BioSphere Putty SYNERGY BIOMEDICAL, LLC
15 M958BMS050RC0 Replacement Cannula BMS-050RC BioSphere MIS SYNERGY BIOMEDICAL, LLC
16 M958BMS050KT0 Kit BMS-050KT BioSphere MIS SYNERGY BIOMEDICAL, LLC
17 M896MAR0FUSE5CC1 MAR0Fuse5cc MAR0Fuse Demineralized Bone Matrix Gel MAR0Fuse ARTERIOCYTE MEDICAL SYSTEMS, INC.
18 M896MAR0FUSE5CC1 MAR0Fuse5cc MAR0Fuse Demineralized Bone Matrix Gel MAR0Fuse ARTERIOCYTE MEDICAL SYSTEMS, INC.
19 M896MAR0FUSE1CC1 MAR0Fuse1cc MAR0Fuse Demineralized Bone Matrix Gel MAR0Fuse ARTERIOCYTE MEDICAL SYSTEMS, INC.
20 M896MAR0FUSE1CC1 MAR0Fuse1cc MAR0Fuse Demineralized Bone Matrix Gel MAR0Fuse ARTERIOCYTE MEDICAL SYSTEMS, INC.
21 M896MAR0FUSE10CC1 MAR0Fuse10cc MAR0FUSE Demineralized Bone Matrix Gel MAR0Fuse ARTERIOCYTE MEDICAL SYSTEMS, INC.
22 M896MAR0FUSE10CC1 MAR0Fuse10cc MAR0FUSE Demineralized Bone Matrix Gel MAR0Fuse ARTERIOCYTE MEDICAL SYSTEMS, INC.
23 M896IQSPPP1100 Paste Mix Plus IQSP-PP-110 Inqu ARTERIOCYTE MEDICAL SYSTEMS, INC.
24 M896IQSPPP1050 Paste Mix Plux IQSP-PP-105 Synthetic bone graft Inqu ARTERIOCYTE MEDICAL SYSTEMS, INC.
25 M896IQSPPP1020 Paste Mix Plus IQSP-PP-102 Synthetic bone graft Inqu ARTERIOCYTE MEDICAL SYSTEMS, INC.
26 M896IQSPPP1010 Paste Mix Plus IQSP-PP-101 Synthetic Bone Graft Inqu ARTERIOCYTE MEDICAL SYSTEMS, INC.
27 M896IQSPMX1500 Matrix IQSP-MX-150 lnQu is a resorbable bone void filler intended to fill bony gaps or voids that a lnQu is a resorbable bone void filler intended to fill bony gaps or voids that are not intrinsic to the stability of the bony structure.InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis). lnQu is indicated for use as a bone graft extender in the spine when combined with bone autograft. These defects may be surgically created or result from traumatic injury to the bone. InQu ARTERIOCYTE MEDICAL SYSTEMS, INC.
28 M896IQSPMX1250 Matrix IQSP-MX-125 lnQu is a resorbable bone void filler intended to fill bony gaps or voids that a lnQu is a resorbable bone void filler intended to fill bony gaps or voids that are not intrinsic to the stability of the bony structure.InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis). lnQu is indicated for use as a bone graft extender in the spine when combined with bone autograft. These defects may be surgically created or result from traumatic injury to the bone. InQu ARTERIOCYTE MEDICAL SYSTEMS, INC.
29 M896IQSPGR1300 Granules IQSP-GR-130 lnQu is a resorbable bone void filler intended to fill bony gaps or voids that a lnQu is a resorbable bone void filler intended to fill bony gaps or voids that are not intrinsic to the stability of the bony structure.InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis). lnQu is indicated for use as a bone graft extender in the spine when combined with bone autograft. These defects may be surgically created or result from traumatic injury to the bone. InQu ARTERIOCYTE MEDICAL SYSTEMS, INC.
30 18257200121878 711015 Osteoconductive Scaffold Strip, 15cc Collage ORTHOFIX INC.
31 18257200121861 711010 Osteoconductive Scaffold Strip 10 cc Collage ORTHOFIX INC.
32 18257200115136 710015 Collage Osteoconductive Scaffold Putty 15cc Collage ORTHOFIX INC.
33 18257200115129 710010 Collage Osteoconductive Scaffold Putty 10 cc Collage ORTHOFIX INC.
34 18257200115112 710005 Collage Osteoconductive Scaffold Putty, 5cc Collage ORTHOFIX INC.
35 15060155711499 910-010Z 910-010Z genex® Bone Graft Substitute is a simple to use synthetic absorbable material de genex® Bone Graft Substitute is a simple to use synthetic absorbable 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 filled syringe and mixing solution which, when combined, provides a mouldablecohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set insitu or placed in the bead mould mat provided to form beads for implantation. When injected the mixturesets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substituteis supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex.genex® Bone Graft Substitute is MR safe. Genex Bone Graft Substitute BIOCOMPOSITES LTD
36 15060155711482 910-005Z 910-005Z genex® Bone Graft Substitute is a simple to use synthetic absorbable material de genex® Bone Graft Substitute is a simple to use synthetic absorbable 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 filled syringe and mixing solution which, when combined, provides a mouldablecohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set insitu or placed in the bead mould mat provided to form beads for implantation. When injected the mixturesets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substituteis supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex.genex® Bone Graft Substitute is MR safe. Genex Bone Graft Substitute BIOCOMPOSITES LTD
37 15060155711475 910-003Z 910-003Z genex® Bone Graft Substitute is a simple to use synthetic absorbable material de genex® Bone Graft Substitute is a simple to use synthetic absorbable 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 filled syringe and mixing solution which, when combined, provides a mouldablecohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set in situ or placed in the bead mould mat provided to form beads for implantation. When injected the mixture sets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substituteis supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex. genex® Bone Graft Substitute is MR safe. Genex Bone Graft Substitute BIOCOMPOSITES LTD
38 15060155711451 620-003 620-003 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
39 15060155711420 910-010 910-010 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
40 15060155711413 910-005 910-005 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
41 15060155711055 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
42 15060155711048 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
43 15060155711031 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
44 15060155711024 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
45 15060155710966 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
46 15060155710959 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
47 15060155710188 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
48 15060155710171 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
49 15060155710164 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
50 15060155710157 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