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 "HTR"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10889981291259 SR-0813-12 SR-0813-12 Trial Rasp, 14 x 13 x 12mm, 7° Lordosis Specials SEASPINE ORTHOPEDICS CORPORATION
2 10889981291242 SR-0813-11 SR-0813-11 Trial Rasp, 14 x 13 x 11mm, 7° Lordosis Specials SEASPINE ORTHOPEDICS CORPORATION
3 10889981291235 SR-0813-10 SR-0813-10 Trial Rasp, 14 x 13 x 10mm, 7° Lordosis Specials SEASPINE ORTHOPEDICS CORPORATION
4 10889981291228 SR-0813-09 SR-0813-09 Trial Rasp, 14 x 13 x 9mm, 7° Lordosis Specials SEASPINE ORTHOPEDICS CORPORATION
5 10889981291211 SR-0813-08 SR-0813-08 Trial Rasp, 14 x 13 x 8mm, 7° Lordosis Specials SEASPINE ORTHOPEDICS CORPORATION
6 10889981291204 SR-0813-07 SR-0813-07 Trial Rasp, 14 x 13 x 7mm, 7° Lordosis Specials SEASPINE ORTHOPEDICS CORPORATION
7 10889981291198 SR-0813-06 SR-0813-06 Trial Rasp, 14 x 13 x 6mm, 7° Lordosis Specials SEASPINE ORTHOPEDICS CORPORATION
8 10889981291181 SR-0813-05 SR-0813-05 Trial Rasp, 14 x 13 x 5mm, 7° Lordosis Specials SEASPINE ORTHOPEDICS CORPORATION
9 10889981290627 SR-0793-1615 SR-0793-1615 Trial Rasp, 43mm x 30mm x 16mm, 15 Specials SEASPINE ORTHOPEDICS CORPORATION
10 10889981290610 SR-0793-1610 SR-0793-1610 Trial Rasp, 43mm x 30mm x 16mm, 10 Specials SEASPINE ORTHOPEDICS CORPORATION
11 10889981290603 SR-0793-1415 SR-0793-1415 Trial Rasp, 43mm x 30mm x 14mm, 15 Specials SEASPINE ORTHOPEDICS CORPORATION
12 10889981290597 SR-0793-1410 SR-0793-1410 Trial Rasp, 43mm x 30mm x 14mm, 10 Specials SEASPINE ORTHOPEDICS CORPORATION
13 10889981290580 SR-0793-1215 SR-0793-1215 Trial Rasp, 43mm x 30mm x 12mm, 15 Specials SEASPINE ORTHOPEDICS CORPORATION
14 10889981290573 SR-0793-1210 SR-0793-1210 Trial Rasp, 43mm x 30mm x 12mm, 10 Specials SEASPINE ORTHOPEDICS CORPORATION
15 10889981290566 SR-0793-1010 SR-0793-1010 Trial Rasp, 43mm x 30mm x 10mm, 10 Specials SEASPINE ORTHOPEDICS CORPORATION
16 10889981276256 SR-0684 SR-0684 Osteophyte Remover, 12mm Specials SEASPINE ORTHOPEDICS CORPORATION
17 10889981276249 SR-0676 SR-0676 Osteophyte Remover, 14mm Specials SEASPINE ORTHOPEDICS CORPORATION
18 10889981276003 SR-0675 SR-0675 Modular Rasp Inserter Specials SEASPINE ORTHOPEDICS CORPORATION
19 10889981263478 SR-0590 SR-0590 Osteophyte Remover Specials SEASPINE ORTHOPEDICS CORPORATION
20 10889981255640 SR-0529 SR-0529 Dual Sided Rasp, Angled at 50mm Specials SEASPINE ORTHOPEDICS CORPORATION
21 10889981246228 SR-0519 SR-0519 Flat Facet Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
22 10889981246211 SR-0518 SR-0518 Domed Facet Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
23 10889981230555 SR-0495 SR-0495 Angled Rasp - 8mm Specials SEASPINE ORTHOPEDICS CORPORATION
24 10889981195625 SR-0461 SR-0461 Angled Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
25 10889981184506 95-6986 95-6986 Single Sided Rasp Anterior Disc Prep SEASPINE ORTHOPEDICS CORPORATION
26 10889981183196 SR-0437-12 SR-0437-12 17x13x12mm Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
27 10889981183189 SR-0437-11 SR-0437-11 17x13x11mm Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
28 10889981183172 SR-0437-10 SR-0437-10 17x13x10mm Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
29 10889981183165 SR-0437-09 SR-0437-09 17x13x09mm Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
30 10889981183158 SR-0437-08 SR-0437-08 17x13x08mm Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
31 10889981183141 SR-0437-07 SR-0437-07 17x13x07mm Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
32 10889981183134 SR-0437-06 SR-0437-06 17x13x06mm Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
33 10889981183127 SR-0437-05 SR-0437-05 17x13x05mm Rasp Specials SEASPINE ORTHOPEDICS CORPORATION
34 10889981183110 SR-0426-12 SR-0426-12 15x13x12mm Rasp, Flat Specials SEASPINE ORTHOPEDICS CORPORATION
35 10889981183103 SR-0426-11 SR-0426-11 15x13x11mm Rasp, Flat Specials SEASPINE ORTHOPEDICS CORPORATION
36 10889981183097 SR-0426-10 SR-0426-10 15x13x10mm Rasp, Flat Specials SEASPINE ORTHOPEDICS CORPORATION
37 10889981183080 SR-0426-09 SR-0426-09 15x13x09mm Rasp, Flat Specials SEASPINE ORTHOPEDICS CORPORATION
38 10889981183073 SR-0426-08 SR-0426-08 15x13x08mm Rasp, Flat Specials SEASPINE ORTHOPEDICS CORPORATION
39 10889981183066 SR-0426-07 SR-0426-07 15x13x07mm Rasp, Flat Specials SEASPINE ORTHOPEDICS CORPORATION
40 10889981183059 SR-0426-06 SR-0426-06 15x13x06mm Rasp, Flat Specials SEASPINE ORTHOPEDICS CORPORATION
41 10889981183042 SR-0426-05 SR-0426-05 15x13x05mm Rasp, Flat Specials SEASPINE ORTHOPEDICS CORPORATION
42 10889981172350 99-0006 99-0006 Rasp Mariner Outrigger SEASPINE ORTHOPEDICS CORPORATION
43 10889981155834 06-70-0618 06-70-0618 Rasp, Angled 8mm Posterior Disc Prep SEASPINE ORTHOPEDICS CORPORATION
44 10889981155827 06-70-0608 06-70-0608 Rasp, Straight 8mm Posterior Disc Prep SEASPINE ORTHOPEDICS CORPORATION
45 10889981154288 06-70-0116 06-70-0116 Rotary Scraper, 16mm Posterior Disc Prep SEASPINE ORTHOPEDICS CORPORATION
46 10889981154271 06-70-0115 06-70-0115 Rotary Scraper, 15mm Posterior Disc Prep SEASPINE ORTHOPEDICS CORPORATION
47 10889981154264 06-70-0114 06-70-0114 Rotary Scraper, 14mm Posterior Disc Prep SEASPINE ORTHOPEDICS CORPORATION
48 10889981154257 06-70-0113 06-70-0113 Rotary Scraper, 13mm Posterior Disc Prep SEASPINE ORTHOPEDICS CORPORATION
49 10889981154240 06-70-0112 06-70-0112 Rotary Scraper, 12mm Posterior Disc Prep SEASPINE ORTHOPEDICS CORPORATION
50 10889981154233 06-70-0111 06-70-0111 Rotary Scraper, 11mm Posterior Disc Prep SEASPINE ORTHOPEDICS CORPORATION