Other products from "NVISION BIOMEDICAL TECHNOLOGIES, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 90814008025315 PLE-015-S PLIF Encoded 10x22 15mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
2 90814008024974 PLE-010-L PLIF Encoded 10x30 10mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
3 90814008024967 PLE-009-L PLIF Encoded 10x30 9mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
4 90814008024950 PLE-008-L PLIF Encoded 10x30 8mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
5 90814008024943 PLE-007-L PLIF Encoded 10x30 7mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
6 90814008024936 PLE-006-L PLIF Encoded 10x30 6mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
7 90814008024929 PLE-615-M PLIF Encoded 10x26 15mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
8 90814008024912 PLE-614-M PLIF Encoded 10x26 14mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
9 90814008024905 PLE-613-M PLIF Encoded 10x26 13mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
10 90814008024899 PLE-612-M PLIF Encoded 10x26 12mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
11 90814008024882 PLE-611-M PLIF Encoded 10x26 11mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
12 90814008024875 PLE-610-M PLIF Encoded 10x26 10mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
13 90814008024868 PLE-609-M PLIF Encoded 10x26 9mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
14 90814008024851 PLE-608-M PLIF Encoded 10x26 8mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
15 90814008024844 PLE-607-M PLIF Encoded 10x26 7mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
16 90814008024837 PLE-015-M PLIF Encoded 10x26 15mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
17 90814008024820 PLE-014-M PLIF Encoded 10x26 14mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
18 90814008024813 PLE-013-M PLIF Encoded 10x26 13mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
19 90814008024806 PLE-012-M PLIF Encoded 10x26 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
20 90814008024790 PLE-011-M PLIF Encoded 10x26 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
21 90814008024783 PLE-010-M PLIF Encoded 10x26 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
22 90814008024776 PLE-009-M PLIF Encoded 10x26 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
23 90814008024769 PLE-008-M PLIF Encoded 10x26 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
24 90814008024752 PLE-007-M PLIF Encoded 10x26 7mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
25 90814008024745 PLE-006-M PLIF Encoded 10x26 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
26 90814008024738 PLE-014-S PLIF Encoded 10x22 14mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
27 90814008024721 PLE-013-S PLIF Encoded 10x22 13mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
28 90814008024714 PLE-012-S PLIF Encoded 10x22 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
29 90814008024707 PLE-011-S PLIF Encoded 10x22 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
30 90814008024691 PLE-010-S PLIF Encoded 10x22 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
31 90814008024684 PLE-009-S PLIF Encoded 10x22 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
32 90814008024677 PLE-008-S PLIF Encoded 10x22 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
33 90814008024660 PLE-007-S PLIF Encoded 10x22 7mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
34 90814008024653 PLE-006-S PLIF Encoded 10x22 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
35 00810005664905 PD-1000C-750 Caddy 7.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy 7.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
36 00810005664899 PD-1000C-650 Caddy 6.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy 6.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
37 00810005662253 PD-1000C-475 Caddy 4.75 Screws. The FOCUS Pedicle Screw System is intended for use in the no Caddy 4.75 Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
38 00810005662246 PD-1000C-SS Caddy Set Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy Set Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
39 00810005662239 PD-1000C-CC Caddy CrossLinks. The FOCUS Pedicle Screw System is intended for use in the non Caddy CrossLinks. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
40 00810005662222 PD-1000C-LR Caddy Lordotic Rods. The FOCUS Pedicle Screw System is intended for use in the Caddy Lordotic Rods. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
41 00810005662215 PD-1000C-SR Caddy Straight Rods. The FOCUS Pedicle Screw System is intended for use in the Caddy Straight Rods. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
42 90814008024981 PLE-011-L PLIF Encoded 10x30 11mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
43 00810005662208 PD-1000C-106 Pedicle Screw Case 4 INSERT 4 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 4 INSERT 4 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
44 00810005662192 PD-1000C-105 Pedicle Screw Case 4 INSERT 3 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 4 INSERT 3 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
45 00810005662185 PD-1000C-104 Pedicle Screw Case 3 INSERT 2 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 3 INSERT 2 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
46 00810005662178 PD-1000C-103 Pedicle Screw Case 3 INSERT 1 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 3 INSERT 1 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
47 00810005662161 PD-1000C-102 Pedicle Screw Case, Instruments. The FOCUS Pedicle Screw System is intended for Pedicle Screw Case, Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
48 00810005662154 PD-1000C-204 Pedicle Screw Case 2 INSERT 3. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 2 INSERT 3. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
49 00810005662147 PD-1000C-211 Pedicle Screw Case 2 Base, Implants. The FOCUS Pedicle Screw System is intended Pedicle Screw Case 2 Base, Implants. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
50 00810005662130 PD-1000C-202 Pedicle Screw Case 1 INSERT 2. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 1 INSERT 2. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
Other products with the same Product Code "ODP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M739FCP12140 FCP1214 Parallel Cage, 12 x 14mm Parallel Cage, 12 x 14mm CAPTIVA SPINE, INC.
2 M739FCP12130 FCP1213 Parallel Cage, 12 x 13mm Parallel Cage, 12 x 13mm CAPTIVA SPINE, INC.
3 M739FCP12120 FCP1212 Parallel Cage, 12 x 12mm Parallel Cage, 12 x 12mm CAPTIVA SPINE, INC.
4 M739FCP1212 FCP1212 Parallel Cage, 12 x 12mm Parallel Cage, 12 x 12mm CAPTIVA SPINE, INC.
5 M739FCP12110 FCP1211 Parallel Cage, 12 x 11mm Parallel Cage, 12 x 11mm CAPTIVA SPINE, INC.
6 M739FCP1211 FCP1211 Parallel Cage, 12 x 11mm Parallel Cage, 12 x 11mm CAPTIVA SPINE, INC.
7 M739FCP12100 FCP1210 Parallel Cage, 12 x 10mm Parallel Cage, 12 x 10mm CAPTIVA SPINE, INC.
8 M739FCP1210 FCP1210 Parallel Cage, 12 x 10mm Parallel Cage, 12 x 10mm CAPTIVA SPINE, INC.
9 M739FCP12090 FCP1209 Parallel Cage, 12 x 9mm Parallel Cage, 12 x 9mm CAPTIVA SPINE, INC.
10 M739FCP1209 FCP1209 Parallel Cage, 12 x 9mm Parallel Cage, 12 x 9mm CAPTIVA SPINE, INC.
11 M739FCP12080 FCP1208 Parallel Cage, 12 x 8mm Parallel Cage, 12 x 8mm CAPTIVA SPINE, INC.
12 M739FCP1208 FCP1208 Parallel Cage, 12 x 8mm Parallel Cage, 12 x 8mm CAPTIVA SPINE, INC.
13 M739FCP12070 FCP1207 Parallel Cage, 12 x 7mm Parallel Cage, 12 x 7mm CAPTIVA SPINE, INC.
14 M739FCP1207 FCP1207 Parallel Cage, 12 x 7mm Parallel Cage, 12 x 7mm CAPTIVA SPINE, INC.
15 M739FCP12060 FCP1206 Parallel Cage, 12 x 6mm Parallel Cage, 12 x 6mm CAPTIVA SPINE, INC.
16 M739FCP1206 FCP1206 Parallel Cage, 12 x 6mm Parallel Cage, 12 x 6mm CAPTIVA SPINE, INC.
17 M739FCP12050 FCP1205 Parallel Cage, 12 x 5mm Parallel Cage, 12 x 5mm CAPTIVA SPINE, INC.
18 M739FCP1205 FCP1205 Parallel Cage, 12 x 5mm Parallel Cage, 12 x 5mm CAPTIVA SPINE, INC.
19 M739FCL12140 FCL1214 Lordotic Cage, 12 x 14mm Lordotic Cage, 12 x 14mm CAPTIVA SPINE, INC.
20 M739FCL12130 FCL1213 Lordotic Cage, 12 x 13mm Lordotic Cage, 12 x 13mm CAPTIVA SPINE, INC.
21 M739FCL12120 FCL1212 Lordotic Cage, 12 x 12mm Lordotic Cage, 12 x 12mm CAPTIVA SPINE, INC.
22 M739FCL1212 FCL1212 Lordotic Cage, 12 x 12mm Lordotic Cage, 12 x 12mm CAPTIVA SPINE, INC.
23 M739FCL12110 FCL1211 Lordotic Cage, 12 x 11mm Lordotic Cage, 12 x 11mm CAPTIVA SPINE, INC.
24 M739FCL1211 FCL1211 Lordotic Cage, 12 x 11mm Lordotic Cage, 12 x 11mm CAPTIVA SPINE, INC.
25 M739FCL12100 FCL1210 Lordotic Cage, 12 x 10mm Lordotic Cage, 12 x 10mm CAPTIVA SPINE, INC.
26 M739FCL1210 FCL1210 Lordotic Cage, 12 x 10mm Lordotic Cage, 12 x 10mm CAPTIVA SPINE, INC.
27 M739FCL12090 FCL1209 Lordotic Cage, 12 x 9mm Lordotic Cage, 12 x 9mm CAPTIVA SPINE, INC.
28 M739FCL1209 FCL1209 Lordotic Cage, 12 x 9mm Lordotic Cage, 12 x 9mm CAPTIVA SPINE, INC.
29 M739FCL12080 FCL1208 Lordotic Cage, 12 x 8mm Lordotic Cage, 12 x 8mm CAPTIVA SPINE, INC.
30 M739FCL1208 FCL1208 Lordotic Cage, 12 x 8mm Lordotic Cage, 12 x 8mm CAPTIVA SPINE, INC.
31 M739FCL12070 FCL1207 Lordotic Cage, 12 x 7mm Lordotic Cage, 12 x 7mm CAPTIVA SPINE, INC.
32 M739FCL1207 FCL1207 Lordotic Cage, 12 x 7mm Lordotic Cage, 12 x 7mm CAPTIVA SPINE, INC.
33 M739FCL12060 FCL1206 Lordotic Cage, 12 x 6mm Lordotic Cage, 12 x 6mm CAPTIVA SPINE, INC.
34 M739FCL1206 FCL1206 Lordotic Cage, 12 x 6mm Lordotic Cage, 12 x 6mm CAPTIVA SPINE, INC.
35 M739FCL12050 FCL1205 Lordotic Cage, 12 x 5mm Lordotic Cage, 12 x 5mm CAPTIVA SPINE, INC.
36 M739FCL1205 FCL1205 Lordotic Cage, 12 x 5mm Lordotic Cage, 12 x 5mm CAPTIVA SPINE, INC.
37 M7391837811120 18378-1112 Lordotic Trial 11/12 x 17mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
38 M7391837809100 18378-0910 Lordotic Trial 9/10 x 17mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
39 M7391837807080 18378-0708 Lordotic Trial 7/8 x 17mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
40 M7391837805060 18378-0506 Lordotic Trial 5/6 x 17mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
41 M7391837711120 18377-1112 Lordotic Trial 11/12 x 17.5mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
42 M7391837709100 18377-0910 Lordotic Trial 9/10 x 17.5mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
43 M7391837707080 18377-0708 Lordotic Trial 7/8 x 17.5mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
44 M7391837705060 18377-0506 Lordotic Trial 5/6 x 17.5mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
45 M7391837611120 18376-1112 Lordotic Trial 11/12 x 16mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
46 M7391837609100 18376-0910 Lordotic Trial 9/10 x 16mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
47 M7391837607080 18376-0708 Lordotic Trial 7/8 x 16mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
48 M7391837605060 18376-0506 Lordotic Trial 5/6 x 16mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
49 M7391837511120 18375-1112 Lordotic Trial 11/12 x 16.5mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.
50 M7391837509100 18375-0910 Lordotic Trial 9/10 x 16.5mm TirboLOX-C Cervical IBFD CAPTIVA SPINE, INC.