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 10852776006017 PD-31-100 PD-31-100 The DTRAX Cervical Cage-T is a single-use, titanium alloy intervertebral implant The DTRAX Cervical Cage-T is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. DTRAX Cervical Cage-T PROVIDENCE MEDICAL TECHNOLOGY, INC.
2 10852776006000 PD-31-200 PD-31-200 The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. DTRAX Cervical Cage-B PROVIDENCE MEDICAL TECHNOLOGY, INC.
3 10840642162028 SW18125-1410 SW18125-1410 Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 10 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
4 10840642162011 SW18125-1409 SW18125-1409 Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 9 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
5 10840642162004 SW18125-1408 SW18125-1408 Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 8 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
6 10840642161991 SW18125-1407 SW18125-1407 Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 7 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
7 10840642161984 SW18125-1406 SW18125-1406 Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 6 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
8 10840642161977 SW18125-1405 SW18125-1405 Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 5 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
9 10840642161960 SW18105-1015 SW18105-1015 Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 10 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
10 10840642161953 SW18105-0915 SW18105-0915 Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 9 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
11 10840642161946 SW18105-0815 SW18105-0815 Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 8 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
12 10840642161939 SW18105-0715 SW18105-0715 Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 7 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
13 10840642161922 SW18105-0615 SW18105-0615 Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 6 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
14 10840642161915 SW18105-0515 SW18105-0515 Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 5 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
15 10840642161908 SW18107-1412 SW18107-1412 Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 12 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
16 10840642161892 SW18107-1411 SW18107-1411 Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 11 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
17 10840642161885 SW18107-1410 SW18107-1410 Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 10 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
18 10840642161878 SW18107-1409 SW18107-1409 Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 9 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
19 10840642161861 SW18107-1408 SW18107-1408 Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 8 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
20 10840642161854 SW18107-1407 SW18107-1407 Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 7 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
21 10840642161847 SW18107-1406 SW18107-1406 Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 6 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
22 10840642161830 SW18107-1405 SW18107-1405 Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 5 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
23 10840642161823 SW18107-1215 SW18107-1215 Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 12 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
24 10840642161816 SW18107-1115 SW18107-1115 Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 11 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
25 10840642161809 SW18107-1015 SW18107-1015 Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 10 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
26 10840642161793 SW18107-0915 SW18107-0915 Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 9 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
27 10840642161786 SW18107-0815 SW18107-0815 Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 8 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
28 10840642161779 SW18107-0715 SW18107-0715 Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 7 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
29 10840642161762 SW18107-0615 SW18107-0615 Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 6 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
30 10840642161755 SW18107-0515 SW18107-0515 Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 5 mm Stronghold® C 3D Titanium Interbody Device System SPINE WAVE, INC.
31 10840642103496 15-6612 15-6612 Spacer 14mm X 16mm X 12mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
32 10840642103489 15-6611 15-6611 Spacer 14mm X 16mm X 11mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
33 10840642103472 15-6610 15-6610 Spacer 14mm X 16mm X 10mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
34 10840642103465 15-6609 15-6609 Spacer 14mm X 16mm X 9mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
35 10840642103458 15-6608 15-6608 Spacer 14mm X 16mm X 8mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
36 10840642103441 15-6607 15-6607 Spacer 14mm X 16mm X 7mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
37 10840642103434 15-6606 15-6606 Spacer 14mm X 16mm X 6mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
38 10840642103427 15-6605 15-6605 Spacer 14mm X 16mm X 5mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
39 10840642103410 15-6012 15-6012 Spacer 14mm X 16mm X 12mm 0deg Accent® Cervical Spacer System SPINE WAVE, INC.
40 10840642103403 15-6011 15-6011 Spacer 14mm X 16mm X 11mm 0deg Accent® Cervical Spacer System SPINE WAVE, INC.
41 10840642103397 15-6010 15-6010 Spacer 14mm X 16mm X 10mm 0deg Accent® Cervical Spacer System SPINE WAVE, INC.
42 10840642103380 15-6009 15-6009 Spacer 14mm X 16mm X 9mm 0deg Accent® Cervical Spacer System SPINE WAVE, INC.
43 10840642103373 15-6008 15-6008 Spacer 14mm X 16mm X 8mm 0deg Accent® Cervical Spacer System SPINE WAVE, INC.
44 10840642103366 15-6007 15-6007 Spacer 14mm X 16mm X 7mm 0deg Accent® Cervical Spacer System SPINE WAVE, INC.
45 10840642103359 15-6006 15-6006 Spacer 14mm X 16mm X 6mm 0deg Accent® Cervical Spacer System SPINE WAVE, INC.
46 10840642103342 15-6005 15-6005 Spacer 14mm X 16mm X 5mm 0deg Accent® Cervical Spacer System SPINE WAVE, INC.
47 10840642103335 15-4612 15-4612 Spacer 12mm X 14mm X 12mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
48 10840642103328 15-4611 15-4611 Spacer 12mm X 14mm X 11mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
49 10840642103311 15-4610 15-4610 Spacer 12mm X 14mm X 10mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.
50 10840642103304 15-4609 15-4609 Spacer 12mm X 14mm X 9mm 6deg Accent® Cervical Spacer System SPINE WAVE, INC.