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 90814008024653 PLE-006-S PLIF Encoded 10x22 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
34 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
35 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
36 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
37 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
38 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
39 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
40 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
41 90814008024981 PLE-011-L PLIF Encoded 10x30 11mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
42 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
43 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
44 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
45 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
46 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
47 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
48 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
49 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
50 00810005662123 PD-1000C-203 Pedicle Screw Case 1 INSERT 1. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 1 INSERT 1. 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 00885074549880 2982844 TRIAL 2982844 8 X 44MM L DISTRACTOR N/A MEDTRONIC SOFAMOR DANEK, INC.
2 00885074549736 2982001 INSERTER 2982001 THREADED N/A MEDTRONIC SOFAMOR DANEK, INC.
3 00885074528038 X0905038 SPACER X0905038 CAPSTONE PEEK 32 x 16 CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
4 00885074502427 X0605269 SPACER X0605269 CAPSTONE PEEK 26 x 7 CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
5 00885074502410 X0605268 SPACER X0605268 CAPSTONE PEEK 26 x 6 CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
6 00885074502397 X0605267 SPACER X0605267 CAPSTONE PEEK 22 x 7 CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
7 00885074502342 X0605249 SPACER X0605249 CAPSTONE PEEK 22 x 6 CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
8 00885074497334 3297101 ACCESSORIES 3297101 IMPLANT INSERTER N/A MEDTRONIC SOFAMOR DANEK, INC.
9 00885074445465 9732430 SOFTWARE, 9732430, SPINE UNIFIED N/A MEDTRONIC NAVIGATION, INC.
10 00885074417509 X0305157 SPACER X0305157 VRTBL XL ADD ON 8DEG18MM PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
11 00885074417486 X0305156 SPACER X0305156 VRTBL XL ADD ON 8DEG16MM PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
12 00885074417417 X0305152 SPACER X0305152 VRBTL XL ADD ON 8DEG8MM PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
13 00885074372778 X1204274 CAGE X1204274 CAPSTONE 14 X 22 X 8 WIDE CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
14 00885074372730 X1204273 CAGE X1204273 CAPSTONE 12 X 22 X 8 WIDE CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
15 00885074372723 X1204272 CAGE X1204272 CAPSTONE 10 X 22 X 8 WIDE CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
16 00885074372693 X1204271 CAGE X1204271 CAPSTONE 8 X 22 X 8 WIDE CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
17 00885074361253 3290114 ACCESSORIES 3290114 TRIAL XL 14MM 8DEG N/A MEDTRONIC SOFAMOR DANEK, INC.
18 00885074360591 3290112 ACCESSORIES 3290112 TRIAL XL 12MM 8DEG N/A MEDTRONIC SOFAMOR DANEK, INC.
19 00885074360584 3290110 ACCESSORIES 3290110 TRIAL XL 10MM 8DEG N/A MEDTRONIC SOFAMOR DANEK, INC.
20 00885074356167 X0205149 SPACER X0205149 CAPSTONE PEEK 26 x 16 CAPSTONE® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
21 00885074240824 3299220 ACCESSORIES 3299220 TRIAL LRG 20MM 12DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
22 00885074240817 3299218 ACCESSORIES 3299218 TRIAL LRG 18MM 12DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
23 00885074240800 3299216 ACCESSORIES 3299216 TRIAL LRG 16MM 12DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
24 00885074240794 3299214 ACCESSORIES 3299214 TRIAL LRG 14MM 12DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
25 00885074240787 3299212 ACCESSORIES 3299212 TRIAL LRG 12MM 12DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
26 00885074240770 3299120 ACCESSORIES 3299120 TRIAL LRG 20MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
27 00885074240763 3299118 ACCESSORIES 3299118 TRIAL LRG 18MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
28 00885074240756 3299116 ACCESSORIES 3299116 TRIAL LRG 16MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
29 00885074240749 3299114 ACCESSORIES 3299114 TRIAL LRG 14MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
30 00885074240732 3299112 ACCESSORIES 3299112 TRIAL LRG 12MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
31 00885074240725 3299110 ACCESSORIES 3299110 TRIAL LRG 10MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
32 00885074240718 3299108 ACCESSORIES 3299108 TRIAL LARGE 8MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
33 00885074240657 3298120 ACCESSORIES 3298120 TRIAL MED 20MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
34 00885074240640 3298118 ACCESSORIES 3298118 TRIAL MED 18MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
35 00885074240633 3298116 ACCESSORIES 3298116 TRIAL MED 16MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
36 00885074240626 3298114 ACCESSORIES 3298114 TRIAL MED 14MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
37 00885074240619 3298112 ACCESSORIES 3298112 TRIAL MED 12MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
38 00885074240602 3298110 ACCESSORIES 3298110 TRIAL MED 10MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
39 00885074240596 3298108 ACCESSORIES 3298108 TRIAL MED 8MM 8DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
40 00885074240589 3297114 ACCESSORIES 3297114 TRIAL SML 14MM 4DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
41 00885074240572 3297112 ACCESSORIES 3297112 TRIAL SML 12MM 4DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
42 00885074240565 3297110 ACCESSORIES 3297110 TRIAL SML 10MM 4DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
43 00885074240558 3297108 ACCESSORIES 3297108 TRIAL SMALL 8MM 4DEG PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
44 00885074088624 2981436 INSTRUMENT 2981436 14X36MM DSTRCTR TRIAL N/A MEDTRONIC SOFAMOR DANEK, INC.
45 00885074088617 2981432 DISTRACTOR/TRIAL 2981432 14 X 32MM N/A MEDTRONIC SOFAMOR DANEK, INC.
46 00885074088600 2981426 INSTRUMENT 2981426 14X26MM DSTRCTR TRIAL N/A MEDTRONIC SOFAMOR DANEK, INC.
47 00885074088594 2981422 INSTRUMENT 2981422 14X22MM DSTRCTR TRIAL N/A MEDTRONIC SOFAMOR DANEK, INC.
48 00885074088570 2981236 INSTRUMENT 2981236 12X36MM DSTRCTR TRIAL N/A MEDTRONIC SOFAMOR DANEK, INC.
49 00885074088556 2981232 INSTRUMENT 2981232 12X32MM DSTRCTR TRIAL N/A MEDTRONIC SOFAMOR DANEK, INC.
50 00885074088549 2981226 INSTRUMENT 2981226 12X26MM DSTRCTR TRIAL N/A MEDTRONIC SOFAMOR DANEK, INC.