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
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No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00810017913251 CI-BLOCK CI-BLOCK Assembly tool Assembly tool ELEVATION SPINE, INC.
2 00810017913244 CI-DRIVER-SP-10 CI-DRIVER-SP-10 Spike Driver, 10mm Spike Driver, 10mm ELEVATION SPINE, INC.
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5 00810017913213 CI-TH5891 CI-TH5891 Trial Head 15x18x10 9 deg. Trial Head 15x18x10 9 deg. ELEVATION SPINE, INC.
6 00810017913206 CI-TH5899 CI-TH5899 Trial Head 15x18x9 9 deg. Trial Head 15x18x9 9 deg. ELEVATION SPINE, INC.
7 00810017913190 CI-TH5898 CI-TH5898 Trial Head 15x18x8 9 deg. Trial Head 15x18x8 9 deg. ELEVATION SPINE, INC.
8 00810017913183 CI-TH5897 CI-TH5897 Trial Head 15x18x7 9 deg. Trial Head 15x18x7 9 deg. ELEVATION SPINE, INC.
9 00810017913176 CI-TH5896 CI-TH5896 Trial Head 15x18x6 9 deg. Trial Head 15x18x6 9 deg. ELEVATION SPINE, INC.
10 00810017913169 CI-TH5895 CI-TH5895 Trial Head 15x18x5 9 deg. Trial Head 15x18x5 9 deg. ELEVATION SPINE, INC.
11 00810017913152 CI-TH5861 CI-TH5861 Trial Head 15x18x10 6 deg. Trial Head 15x18x10 6 deg. ELEVATION SPINE, INC.
12 00810017913145 CI-TH5869 CI-TH5869 Trial Head 15x18x9 6 deg. Trial Head 15x18x9 6 deg. ELEVATION SPINE, INC.
13 00810017913138 CI-TH5868 CI-TH5868 Trial Head 15x18x8 6 deg. Trial Head 15x18x8 6 deg. ELEVATION SPINE, INC.
14 00810017913121 CI-TH5867 CI-TH5867 Trial Head 15x18x7 6 deg. Trial Head 15x18x7 6 deg. ELEVATION SPINE, INC.
15 00810017913114 CI-TH5866 CI-TH5866 Trial Head 15x18x6 6 deg. Trial Head 15x18x6 6 deg. ELEVATION SPINE, INC.
16 00810017913107 CI-TH5865 CI-TH5865 Trial Head 15x18x5 6 deg. Trial Head 15x18x5 6 deg. ELEVATION SPINE, INC.
17 00810017913091 CI-TH5801 CI-TH5801 Trial Head 15x18x10 0 deg. Trial Head 15x18x10 0 deg. ELEVATION SPINE, INC.
18 00810017913084 CI-TH5809 CI-TH5809 Trial Head 15x18x9 0 deg. Trial Head 15x18x9 0 deg. ELEVATION SPINE, INC.
19 00810017913077 CI-TH5808 CI-TH5808 Trial Head 15x18x8 0 deg. Trial Head 15x18x8 0 deg. ELEVATION SPINE, INC.
20 00810017913060 CI-TH5807 CI-TH5807 Trial Head 15x18x7 0 deg. Trial Head 15x18x7 0 deg. ELEVATION SPINE, INC.
21 00810017913053 CI-TH5806 CI-TH5806 Trial Head 15x18x6 0 deg. Trial Head 15x18x6 0 deg. ELEVATION SPINE, INC.
22 00810017913046 CI-TH5805 CI-TH5805 Trial Head 15x18x5 0 deg. Trial Head 15x18x5 0 deg. ELEVATION SPINE, INC.
23 00810017913039 CI-TH4591 CI-TH4591 Trial Head 14x15x10 9 deg. Trial Head 14x15x10 9 deg. ELEVATION SPINE, INC.
24 00810017913022 CI-TH4599 CI-TH4599 Trial Head 14x15x9 9 deg. Trial Head 14x15x9 9 deg. ELEVATION SPINE, INC.
25 00810017913015 CI-TH4598 CI-TH4598 Trial Head 14x15x8 9 deg. Trial Head 14x15x8 9 deg. ELEVATION SPINE, INC.
26 00810017913008 CI-TH4597 CI-TH4597 Trial Head 14x15x7 9 deg. Trial Head 14x15x7 9 deg. ELEVATION SPINE, INC.
27 00810017912995 CI-TH4596 CI-TH4596 Trial Head 14x15x6 9 deg. Trial Head 14x15x6 9 deg. ELEVATION SPINE, INC.
28 00810017912988 CI-TH4595 CI-TH4595 Trial Head 14x15x5 9 deg. Trial Head 14x15x5 9 deg. ELEVATION SPINE, INC.
29 00810017912971 CI-TH4561 CI-TH4561 Trial Head 14x15x10 6 deg. Trial Head 14x15x10 6 deg. ELEVATION SPINE, INC.
30 00810017912964 CI-TH4569 CI-TH4569 Trial Head 14x15x9 6 deg. Trial Head 14x15x9 6 deg. ELEVATION SPINE, INC.
31 00810017912957 CI-TH4568 CI-TH4568 Trial Head 14x15x8 6 deg. Trial Head 14x15x8 6 deg. ELEVATION SPINE, INC.
32 00810017912940 CI-TH4567 CI-TH4567 Trial Head 14x15x7 6 deg. Trial Head 14x15x7 6 deg. ELEVATION SPINE, INC.
33 00810017912933 CI-TH4566 CI-TH4566 Trial Head 14x15x6 6 deg. Trial Head 14x15x6 6 deg. ELEVATION SPINE, INC.
34 00810017912926 CI-TH4565 CI-TH4565 Trial Head 14x15x5 6 deg. Trial Head 14x15x5 6 deg. ELEVATION SPINE, INC.
35 00810017912919 CI-TH4501 CI-TH4501 Trial Head 14x15x10 0 deg. Trial Head 14x15x10 0 deg. ELEVATION SPINE, INC.
36 00810017912902 CI-TH4509 CI-TH4509 Trial Head 14x15x9 0 deg. Trial Head 14x15x9 0 deg. ELEVATION SPINE, INC.
37 00810017912896 CI-TH4508 CI-TH4508 Trial Head 14x15x8 0 deg. Trial Head 14x15x8 0 deg. ELEVATION SPINE, INC.
38 00810017912889 CI-TH4507 CI-TH4507 Trial Head 14x15x7 0 deg. Trial Head 14x15x7 0 deg. ELEVATION SPINE, INC.
39 00810017912872 CI-TH4506 CI-TH4506 Trial Head 14x15x6 0 deg. Trial Head 14x15x6 0 deg. ELEVATION SPINE, INC.
40 00810017912865 CI-TH4505 CI-TH4505 Trial Head 14x15x5 0 deg. Trial Head 14x15x5 0 deg. ELEVATION SPINE, INC.
41 00810017912858 CI-TH4791 CI-TH4791 Trial Head 14x17x10 9 deg. Trial Head 14x17x10 9 deg. ELEVATION SPINE, INC.
42 00810017912841 CI-TH4799 CI-TH4799 Trial Head 14x17x9 9 deg. Trial Head 14x17x9 9 deg. ELEVATION SPINE, INC.
43 00810017912834 CI-TH4798 CI-TH4798 Trial Head 14x17x8 9 deg. Trial Head 14x17x8 9 deg. ELEVATION SPINE, INC.
44 00810017912827 CI-TH4797 CI-TH4797 Trial Head 14x17x7 9 deg. Trial Head 14x17x7 9 deg. ELEVATION SPINE, INC.
45 00810017912810 CI-TH4796 CI-TH4796 Trial Head 14x17x6 9 deg. Trial Head 14x17x6 9 deg. ELEVATION SPINE, INC.
46 00810017912803 CI-TH4795 CI-TH4795 Trial Head 14x17x5 9 deg. Trial Head 14x17x5 9 deg. ELEVATION SPINE, INC.
47 00810017912797 CI-TH4761 CI-TH4761 Trial Head 14x17x10 6 deg. Trial Head 14x17x10 6 deg. ELEVATION SPINE, INC.
48 00810017912780 CI-TH4769 CI-TH4769 Trial Head 14x17x9 6 deg. Trial Head 14x17x9 6 deg. ELEVATION SPINE, INC.
49 00810017912773 CI-TH4768 CI-TH4768 Trial Head 14x17x8 6 deg. Trial Head 14x17x8 6 deg. ELEVATION SPINE, INC.
50 00810017912766 CI-TH4767 CI-TH4767 Trial Head 14x17x7 6 deg. Trial Head 14x17x7 6 deg. ELEVATION SPINE, INC.