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 "KWQ"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10840642167092 15-5478 15-5478 4 Level Plate, 78 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
2 10840642167085 15-5474 15-5474 4 Level Plate, 74 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
3 10840642168051 15-5936 15-5936 Variable Self-Tapping Screw, ø4.35 mm X 16 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
4 10840642168037 15-5934 15-5934 Variable Self-Tapping Screw, ø4.35 mm X 14 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
5 10840642168013 15-5932 15-5932 Variable Self-Tapping Screw, ø4.35 mm X 12 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
6 10840642167931 15-5916 15-5916 Variable Self-Tapping Screw, ø4.0 mm X 16 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
7 10840642167917 15-5914 15-5914 Variable Self-Tapping Screw, ø4.0 mm X 14 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
8 10840642167894 15-5912 15-5912 Variable Self-Tapping Screw, ø4.0 mm X 12 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
9 10840642167863 15-5842 15-5842 Variable Self-Drilling Screw, ø4.35 mm X 22 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
10 10840642167856 15-5840 15-5840 Variable Self-Drilling Screw, ø4.35 mm X 20 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
11 10840642167832 15-5838 15-5838 Variable Self-Drilling Screw, ø4.35 mm X 18 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
12 10840642167818 15-5836 15-5836 Variable Self-Drilling Screw, ø4.35 mm X 16 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
13 10840642167795 15-5834 15-5834 Variable Self-Drilling Screw, ø4.35 mm X 14 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
14 10840642167771 15-5832 15-5832 Variable Self-Drilling Screw, ø4.35 mm X 12 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
15 10840642167757 15-5830 15-5830 Variable Self-Drilling Screw, ø4.35 mm X 10 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
16 10840642167740 15-5822 15-5822 Variable Self-Drilling Screw, ø4.0 mm X 22 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
17 10840642167733 15-5820 15-5820 Variable Self-Drilling Screw, ø4.0 mm X 20 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
18 10840642167719 15-5818 15-5818 Variable Self-Drilling Screw, ø4.0 mm X 18 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
19 10840642167696 15-5816 15-5816 Variable Self-Drilling Screw, ø4.0 mm X 16 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
20 10840642167672 15-5814 15-5814 Variable Self-Drilling Screw, ø4.0 mm X 14 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
21 10840642167658 15-5812 15-5812 Variable Self-Drilling Screw, ø4.0 mm X 12 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
22 10840642167634 15-5810 15-5810 Variable Self-Drilling Screw, ø4.0 mm X 10 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
23 10840642167573 15-5736 15-5736 Fixed Self-Tapping Screw, ø4.35 mm X 16 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
24 10840642167559 15-5734 15-5734 Fixed Self-Tapping Screw, ø4.35 mm X 14 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
25 10840642167535 15-5732 15-5732 Fixed Self-Tapping Screw, ø4.35 mm X 12 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
26 10840642167450 15-5716 15-5716 Fixed Self-Tapping Screw, ø4.0 mm X 16 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
27 10840642167436 15-5714 15-5714 Fixed Self-Tapping Screw, ø4.0 mm X 14 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
28 10840642167412 15-5712 15-5712 Fixed Self-Tapping Screw, ø4.0 mm X 12 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
29 10840642167382 15-5642 15-5642 Fixed Self-Drilling Screw, ø4.35 mm X 22 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
30 10840642167375 15-5640 15-5640 Fixed Self-Drilling Screw, ø4.35 mm X 20 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
31 10840642167351 15-5638 15-5638 Fixed Self-Drilling Screw, ø4.35 mm X 18 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
32 10840642167337 15-5636 15-5636 Fixed Self-Drilling Screw, ø4.35 mm X 16 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
33 10840642167313 15-5634 15-5634 Fixed Self-Drilling Screw, ø4.35 mm X 14 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
34 10840642167290 15-5632 15-5632 Fixed Self-Drilling Screw, ø4.35 mm X 12 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
35 10840642167276 15-5630 15-5630 Fixed Self-Drilling Screw, ø4.35 mm X 10 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
36 10840642167269 15-5622 15-5622 Fixed Self-Drilling Screw, ø4.0 mm X 22 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
37 10840642167252 15-5620 15-5620 Fixed Self-Drilling Screw, ø4.0 mm X 20 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
38 10840642167238 15-5618 15-5618 Fixed Self-Drilling Screw, ø4.0 mm X 18 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
39 10840642167214 15-5616 15-5616 Fixed Self-Drilling Screw, ø4.0 mm X 16 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
40 10840642167191 15-5614 15-5614 Fixed Self-Drilling Screw, ø4.0 mm X 14 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
41 10840642167177 15-5612 15-5612 Fixed Self-Drilling Screw, ø4.0 mm X 12 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
42 10840642167153 15-5610 15-5610 Fixed Self-Drilling Screw, ø4.0 mm X 10 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
43 10840642167146 15-5591 15-5591 5 Level Plate, 91 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
44 10840642167139 15-5586 15-5586 5 Level Plate, 86 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
45 10840642167122 15-5581 15-5581 5 Level Plate, 81 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
46 10840642167115 15-5576 15-5576 5 Level Plate, 76 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
47 10840642167108 15-5571 15-5571 5 Level Plate, 71 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
48 10840642167078 15-5470 15-5470 4 Level Plate, 70 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
49 10840642167061 15-5466 15-5466 4 Level Plate, 66 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.
50 10840642167054 15-5462 15-5462 4 Level Plate, 62 mm Defender™ Anterior Cervical Plate System SPINE WAVE, INC.