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 "MAX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10889981301095 SR-0886 SR-0886 Regatta Compound Angle Inserter, Caudal Specials SEASPINE ORTHOPEDICS CORPORATION
2 10889981301088 SR-0885 SR-0885 Regatta Compound Angle Inserter, Cranial Specials SEASPINE ORTHOPEDICS CORPORATION
3 10889981298807 RA1-200420 RA1-200420 4 Hole Anterior Plate, 20mm Meridian SEASPINE ORTHOPEDICS CORPORATION
4 10889981298791 RA1-200418 RA1-200418 4 Hole Anterior Plate, 18mm Meridian SEASPINE ORTHOPEDICS CORPORATION
5 10889981298784 RA1-200416 RA1-200416 4 Hole Anterior Plate, 16mm Meridian SEASPINE ORTHOPEDICS CORPORATION
6 10889981298777 RA1-200414 RA1-200414 4 Hole Anterior Plate, 14mm Meridian SEASPINE ORTHOPEDICS CORPORATION
7 10889981298760 RA1-200412 RA1-200412 4 Hole Anterior Plate, 12mm Meridian SEASPINE ORTHOPEDICS CORPORATION
8 10889981298753 RA1-200410 RA1-200410 4 Hole Anterior Plate, 10mm Meridian SEASPINE ORTHOPEDICS CORPORATION
9 10889981298746 RA1-200220 RA1-200220 2 Hole Anterior Plate, 20mm Meridian SEASPINE ORTHOPEDICS CORPORATION
10 10889981298739 RA1-200218 RA1-200218 2 Hole Anterior Plate, 18mm Meridian SEASPINE ORTHOPEDICS CORPORATION
11 10889981298722 RA1-200216 RA1-200216 2 Hole Anterior Plate, 16mm Meridian SEASPINE ORTHOPEDICS CORPORATION
12 10889981298715 RA1-200214 RA1-200214 2 Hole Anterior Plate, 14mm Meridian SEASPINE ORTHOPEDICS CORPORATION
13 10889981298708 RA1-200212 RA1-200212 2 Hole Anterior Plate, 12mm Meridian SEASPINE ORTHOPEDICS CORPORATION
14 10889981298692 RA1-200210 RA1-200210 2 Hole Anterior Plate, 10mm Meridian SEASPINE ORTHOPEDICS CORPORATION
15 10889981295257 RA1-000222 RA1-000222 Anterior Plate Locking Cover, 22mm Meridian SEASPINE ORTHOPEDICS CORPORATION
16 10889981294854 RA1-341833 RA1-341833 Interbody, 43mm x 30mm x 18mm, 33 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
17 10889981294847 RA1-341830 RA1-341830 Interbody, 43mm x 30mm x 18mm, 30 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
18 10889981294830 RA1-341825 RA1-341825 Interbody, 43mm x 30mm x 18mm, 25 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
19 10889981294823 RA1-341820 RA1-341820 Interbody, 43mm x 30mm x 18mm, 20 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
20 10889981294816 RA1-341815 RA1-341815 Interbody, 43mm x 30mm x 18mm, 15 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
21 10889981294809 RA1-341810 RA1-341810 Interbody, 43mm x 30mm x 18mm, 10 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
22 10889981294793 RA1-341625 RA1-341625 Interbody, 43mm x 30mm x 16mm, 25 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
23 10889981294786 RA1-341620 RA1-341620 Interbody, 43mm x 30mm x 16mm, 20 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
24 10889981294779 RA1-341615 RA1-341615 Interbody, 43mm x 30mm x 16mm, 15 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
25 10889981294762 RA1-341610 RA1-341610 Interbody, 43mm x 30mm x 16mm, 10 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
26 10889981294755 RA1-341420 RA1-341420 Interbody, 43mm x 30mm x 14mm, 20 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
27 10889981294748 RA1-341415 RA1-341415 Interbody, 43mm x 30mm x 14mm, 15 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
28 10889981294731 RA1-341410 RA1-341410 Interbody, 43mm x 30mm x 14mm, 10 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
29 10889981294724 RA1-341220 RA1-341220 Interbody, 43mm x 30mm x 12mm, 20 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
30 10889981294717 RA1-341215 RA1-341215 Interbody, 43mm x 30mm x 12mm, 15 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
31 10889981294700 RA1-341210 RA1-341210 Interbody, 43mm x 30mm x 12mm, 10 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
32 10889981294694 RA1-341015 RA1-341015 Interbody, 43mm x 30mm x 10mm, 15 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
33 10889981294687 RA1-341010 RA1-341010 Interbody, 43mm x 30mm x 10mm, 10 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
34 10889981294670 RA1-340810 RA1-340810 Interbody, 43mm x 30mm x 8mm, 10 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
35 10889981294663 RA1-332033 RA1-332033 Interbody, 39mm x 30mm x 20mm, 33 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
36 10889981294656 RA1-332030 RA1-332030 Interbody, 39mm x 30mm x 20mm, 30 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
37 10889981294649 RA1-332025 RA1-332025 Interbody, 39mm x 30mm x 20mm, 25 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
38 10889981294632 RA1-332020 RA1-332020 Interbody, 39mm x 30mm x 20mm, 20 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
39 10889981294625 RA1-332015 RA1-332015 Interbody, 39mm x 30mm x 20mm, 15 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
40 10889981294618 RA1-332010 RA1-332010 Interbody, 39mm x 30mm x 20mm, 10 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
41 10889981294601 RA1-331833 RA1-331833 Interbody, 39mm x 30mm x 18mm, 33 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
42 10889981294595 RA1-331830 RA1-331830 Interbody, 39mm x 30mm x 18mm, 30 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
43 10889981294588 RA1-331825 RA1-331825 Interbody, 39mm x 30mm x 18mm, 25 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
44 10889981294571 RA1-331820 RA1-331820 Interbody, 39mm x 30mm x 18mm, 20 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
45 10889981294564 RA1-331815 RA1-331815 Interbody, 39mm x 30mm x 18mm, 15 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
46 10889981294557 RA1-331810 RA1-331810 Interbody, 39mm x 30mm x 18mm, 10 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
47 10889981294540 RA1-331625 RA1-331625 Interbody, 39mm x 30mm x 16mm, 25 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
48 10889981294533 RA1-331620 RA1-331620 Interbody, 39mm x 30mm x 16mm, 20 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
49 10889981294526 RA1-331615 RA1-331615 Interbody, 39mm x 30mm x 16mm, 15 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION
50 10889981294519 RA1-331610 RA1-331610 Interbody, 39mm x 30mm x 16mm, 10 Deg Meridian SEASPINE ORTHOPEDICS CORPORATION