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 00681490992107 9690853 SCREW 9690853 M10 RED BREAK OFF SET CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
2 00681490991261 9680853 M10 REDUCTION BREAK OFF SCREW CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
3 00681490919715 8370030 ROD 8370030 TSR2D PCUT BENT 30MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
4 00681490911894 8281246 3D SCREW 8281246 SET 3BDL HEX TI TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
5 00681490909877 8370100 ROD 8370100 TSR2D PCUT BENT 100MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
6 00681490909860 8370095 ROD 8370095 TSR2D PCUT BENT 95MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
7 00681490909853 8370090 ROD 8370090 TSR2D PCUT BENT 90MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
8 00681490909839 8370080 ROD 8370080 TSR2D PCUT BENT 80MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
9 00681490909815 8370070 ROD 8370070 TSR2D PCUT BENT 70MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
10 00681490909808 8370065 ROD 8370065 TSR2D PCUT BENT 65MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
11 00681490909785 8370060 ROD 8370060 TSR2D PCUT BENT 60MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
12 00681490909778 8370055 ROD 8370055 TSR2D PCUT BENT 55MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
13 00681490909761 8370050 ROD 8370050 TSR2D PCUT BENT 50MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
14 00681490909754 8370045 ROD 8370045 TSR2D PCUT BENT45MM X 5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
15 00681490909747 8370040 ROD 8370040 TSR2D PCUT BENT 40MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
16 00681490909723 8370035 ROD 8370035 TSR2D PCUT BENT 35MMX5.5MM TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
17 00681490909662 8379120C 3D CONNECTOR 8379120C 3MM OFFSET 5.5 TI TSRH® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
18 00681490903240 8574535 CDH M8 FAS 4.5 X 35 CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
19 00681490903233 8574530 CDH M8 FAS 4.5 X 30 CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
20 00681490903226 8574525 CDH M8 FAS 4.5 X 25 CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
21 00681490903202 8570130 EXTENDED BODY HOOK CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
22 00681490903196 8570142 OFFSET HOOK LEFT CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
23 00681490903189 8570140 OFFSET HOOK RIGHT CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
24 00681490903172 8570052 THORACIC HOOK CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
25 00681490903165 8570018 WIDE BLADE LRG THROAT HOOK CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
26 00681490903158 8570020 THIN BLADE HOOK CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
27 00681490903141 8570024 ANGLED HOOK CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
28 00681490903134 8570010 WIDE BLADE HOOK CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
29 00681490903127 8570002 PEDICLE HOOK CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
30 00681490902977 8579018 CROSSLINK 8579018 4.5 LP 2.15 2.95 CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
31 00681490902960 8579017 CROSSLINK 8579017 4.5 LP 1.75 2.15 CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
32 00681490902953 8579016 CROSSLINK 8579016 4.5 LP 1.55 1.75 CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
33 00681490902946 8579015 CROSSLINK 8579015 4.5 LP 1.50038MM CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
34 00681490902717 8698505 STAPLE 8698505 CDH M8 DUAL ROD LG RO CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
35 00681490902700 8698504 STAPLE 8698504 CDH M8 DUAL ROD LG CA CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
36 00681490902694 8698503 STAPLE 8698503 CDH M8 DUAL ROD MD RO CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
37 00681490902687 8698502 STAPLE 8698502 CDH M8 DUAL ROD MD CA CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
38 00681490902663 8698501 STAPLE 8698501 CDH M8 DUAL ROD SM RO CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
39 00681490902656 8698500 STAPLE 8698500 CDH M8 DUAL ROD SM CA CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
40 00681490635646 Y8692645 LONG ARM M8 MAS 6.5 L45 CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
41 00681490540926 8799170 PLATE 8799170 ZEPHIR 70MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.
42 00681490540919 8799167 PLATE 8799167 ZEPHIR 67.5MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.
43 00681490540902 8799165 PLATE 8799165 ZEPHIR 65MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.
44 00681490540896 8799162 PLATE 8799162 ZEPHIR 62.5MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.
45 00681490540889 8799160 PLATE 8799160 ZEPHIR 60MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.
46 00681490540872 8799157 PLATE 8799157 ZEPHIR 57.5MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.
47 00681490540865 8799155 PLATE 8799155 ZEPHIR 55MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.
48 00681490540858 8799152 PLATE 8799152 ZEPHIR 52.5MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.
49 00681490540834 8799150 PLATE 8799150 ZEPHIR 50MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.
50 00681490540810 8799147 PLATE 8799147ZEPHIR 47.5MM TI ZEPHIR® Anterior Cervical System MEDTRONIC SOFAMOR DANEK, INC.