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 90814008024813 PLE-013-M PLIF Encoded 10x26 13mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
18 90814008024806 PLE-012-M PLIF Encoded 10x26 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
19 90814008024790 PLE-011-M PLIF Encoded 10x26 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
20 90814008024783 PLE-010-M PLIF Encoded 10x26 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
21 90814008024776 PLE-009-M PLIF Encoded 10x26 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
22 90814008024769 PLE-008-M PLIF Encoded 10x26 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
23 90814008024752 PLE-007-M PLIF Encoded 10x26 7mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
24 90814008024745 PLE-006-M PLIF Encoded 10x26 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
25 90814008024738 PLE-014-S PLIF Encoded 10x22 14mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
26 90814008024721 PLE-013-S PLIF Encoded 10x22 13mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
27 90814008024714 PLE-012-S PLIF Encoded 10x22 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
28 90814008024707 PLE-011-S PLIF Encoded 10x22 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
29 90814008024691 PLE-010-S PLIF Encoded 10x22 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
30 90814008024684 PLE-009-S PLIF Encoded 10x22 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
31 90814008024677 PLE-008-S PLIF Encoded 10x22 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
32 90814008024660 PLE-007-S PLIF Encoded 10x22 7mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
33 90814008024653 PLE-006-S PLIF Encoded 10x22 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
34 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
35 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
36 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
37 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
38 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
39 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
40 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
41 90814008024981 PLE-011-L PLIF Encoded 10x30 11mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
42 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
43 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
44 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
45 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
46 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
47 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
48 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
49 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
50 00810005662123 PD-1000C-203 Pedicle Screw Case 1 INSERT 1. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 1 INSERT 1. 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 "MAX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10840642162110 SW19106-3016 SW19106-3016 Curved Titanium Cage - Lordotic 30 mm x 16 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
2 10840642162103 SW19106-3015 SW19106-3015 Curved Titanium Cage - Lordotic 30 mm x 15 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
3 10840642162097 SW19106-3014 SW19106-3014 Curved Titanium Cage - Lordotic 30 mm x 14 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
4 10840642162080 SW19106-3013 SW19106-3013 Curved Titanium Cage - Lordotic 30 mm x 13 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
5 10840642162073 SW19106-3012 SW19106-3012 Curved Titanium Cage - Lordotic 30 mm x 12 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
6 10840642162066 SW19106-3011 SW19106-3011 Curved Titanium Cage - Lordotic 30 mm x 11 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
7 10840642162059 SW19106-3010 SW19106-3010 Curved Titanium Cage - Lordotic 30 mm x 10 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
8 10840642162042 SW19106-3009 SW19106-3009 Curved Titanium Cage - Lordotic 30 mm x 9 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
9 10840642162035 SW19106-3008 SW19106-3008 Curved Titanium Cage - Lordotic 30 mm x 8 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
10 10840642161748 SW19159-2514 SW19159-2514 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
11 10840642161731 SW19159-2513 SW19159-2513 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
12 10840642161724 SW19159-2512 SW19159-2512 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
13 10840642161717 SW19159-2511 SW19159-2511 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
14 10840642161700 SW19159-2510 SW19159-2510 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
15 10840642161694 SW19159-2509 SW19159-2509 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
16 10840642161687 SW19159-2508 SW19159-2508 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
17 10840642161670 SW19159-2507 SW19159-2507 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
18 10840642161663 SW19159-2214 SW19159-2214 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
19 10840642161656 SW19159-2213 SW19159-2213 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
20 10840642161649 SW19159-2212 SW19159-2212 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
21 10840642161632 SW19159-2211 SW19159-2211 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
22 10840642161625 SW19159-2210 SW19159-2210 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
23 10840642161618 SW19159-2209 SW19159-2209 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
24 10840642161601 SW19159-2208 SW19159-2208 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
25 10840642161595 SW19159-2207 SW19159-2207 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
26 10840642161588 SW19169-3014 SW19169-3014 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
27 10840642161571 SW19169-3013 SW19169-3013 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
28 10840642161564 SW19169-3012 SW19169-3012 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
29 10840642161557 SW19169-3011 SW19169-3011 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
30 10840642161540 SW19169-3010 SW19169-3010 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
31 10840642161533 SW19169-3009 SW19169-3009 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
32 10840642161526 SW19169-3008 SW19169-3008 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
33 10840642161519 SW19169-3007 SW19169-3007 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
34 10840642161502 SW19109-3014 SW19109-3014 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
35 10840642161496 SW19109-3013 SW19109-3013 Lumbar Titanium Cage – Convex 9.5 mm x 30 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
36 10840642161489 SW19109-3012 SW19109-3012 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
37 10840642161472 SW19109-3011 SW19109-3011 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
38 10840642161465 SW19109-3010 SW19109-3010 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
39 10840642161458 SW19109-3009 SW19109-3009 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
40 10840642161441 SW19109-3008 SW19109-3008 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
41 10840642161434 SW19109-3007 SW19109-3007 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
42 10840642161427 SW19169-2514 SW19169-2514 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
43 10840642161410 SW19169-2513 SW19169-2513 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
44 10840642161403 SW19169-2512 SW19169-2512 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
45 10840642161397 SW19169-2511 SW19169-2511 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
46 10840642161380 SW19169-2510 SW19169-2510 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
47 10840642161373 SW19169-2509 SW19169-2509 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
48 10840642161366 SW19169-2508 SW19169-2508 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
49 10840642161359 SW19169-2507 SW19169-2507 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
50 10840642161342 SW19109-2514 SW19109-2514 Lumbar Titanium Cage - Convex 9.5 mm x 25 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.