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 90814008024806 PLE-012-M PLIF Encoded 10x26 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
19 90814008024790 PLE-011-M PLIF Encoded 10x26 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
20 90814008024783 PLE-010-M PLIF Encoded 10x26 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
21 90814008024776 PLE-009-M PLIF Encoded 10x26 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
22 90814008024769 PLE-008-M PLIF Encoded 10x26 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
23 90814008024752 PLE-007-M PLIF Encoded 10x26 7mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
24 90814008024745 PLE-006-M PLIF Encoded 10x26 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
25 90814008024738 PLE-014-S PLIF Encoded 10x22 14mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
26 90814008024721 PLE-013-S PLIF Encoded 10x22 13mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
27 90814008024714 PLE-012-S PLIF Encoded 10x22 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
28 90814008024707 PLE-011-S PLIF Encoded 10x22 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
29 90814008024691 PLE-010-S PLIF Encoded 10x22 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
30 90814008024684 PLE-009-S PLIF Encoded 10x22 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
31 90814008024677 PLE-008-S PLIF Encoded 10x22 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
32 90814008024660 PLE-007-S PLIF Encoded 10x22 7mm 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 00763000552435 981000007 SHAFT 981000007 ANTERIOR PARA/LORD 7N Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
2 00763000552428 981000006 SHAFT 981000006 ANTERIOR PARA/LORD 6N Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
3 00763000510794 46841223 MINIPLATE 46841223 12X23MM OFFSET 2.5MM Anteralign Spinal System with Titan nanoLock Surface technology MEDTRONIC SOFAMOR DANEK, INC.
4 00763000510787 46841220 MINIPLATE 46841220 12X20MM OFFSET 2.5MM Anteralign Spinal System with Titan nanoLock Surface technology MEDTRONIC SOFAMOR DANEK, INC.
5 00763000510770 46831223 MINIPLATE 46831223 LARGE 12X23MM Anteralign Spinal System with Titan nanoLock Surface technology MEDTRONIC SOFAMOR DANEK, INC.
6 00763000510763 46831220 MINIPLATE 46831220 SMALL 12X20MM Anteralign Spinal System with Titan nanoLock Surface technology MEDTRONIC SOFAMOR DANEK, INC.
7 00763000508821 4675050 BONE SCREW 4675050 LS 5.0X50MM Anteralign Spinal System with Titan nanoLock Surface technology MEDTRONIC SOFAMOR DANEK, INC.
8 00763000508814 4675040 BONE SCREW 4675040 LS 5.0X40MM Anteralign Spinal System with Titan nanoLock Surface technology MEDTRONIC SOFAMOR DANEK, INC.
9 00763000508807 4675030 BONE SCREW 4675030 LS 5.0X30MM Anteralign Spinal System with Titan nanoLock Surface technology MEDTRONIC SOFAMOR DANEK, INC.
10 00763000508791 4675020 BONE SCREW 4675020 LS 5.0X20MM Anteralign Spinal System with Titan nanoLock Surface technology MEDTRONIC SOFAMOR DANEK, INC.
11 00763000466084 981000003 SHAFT 981000003 ANTERIOR ANT/POST Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
12 00763000466077 981000002 SHAFT 981000002 ANTERIOR PARA/LORD Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
13 00763000466060 981000001 INSERTER 981000001 STRAIGHT INSERTER Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
14 00763000465919 981027725 SPACER 981027725 10MM ANT EXPANDABLE LG Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
15 00763000465902 981027722 SPACER 981027722 6MM ANT EXPANDABLE LG Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
16 00763000465896 981025525 SPACER 981025525 10MM ANT EXPANDABLE MD Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
17 00763000465889 981025522 SPACER 981025522 6MM ANT EXPANDABLE MD Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
18 00763000465872 981023325 SPACER 981023325 10MM ANT EXPANDABLE SM Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
19 00763000465865 981023322 SPACER 981023322 6MM ANT EXPANDABLE SM Catalyft™ LS Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
20 00763000385941 X0220058 INSERTER X0220058 PIVOX 25 DEGREE PIVOX™ Oblique Lateral Spinal System MEDTRONIC SOFAMOR DANEK, INC.
21 00763000381110 9730605 INST 9730605 FRAME REF SM PASSIVE SP N/A MEDTRONIC NAVIGATION, INC.
22 00763000356811 9735159 INTS KIT 9735159 SURETRAK II MED FIGHTER N/A MEDTRONIC NAVIGATION, INC.
23 00763000356804 9735158 INST KIT 9735158 SURETRAK II MED CLAMP N/A MEDTRONIC NAVIGATION, INC.
24 00763000352097 RBT071675 TAP RBT071675 RG SABER 7.5 AWL-TIP LONG CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
25 00763000352080 RBT071665 TAP RBT071665 RG SABER 6.5 AWL-TIP LONG CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
26 00763000352073 RBT071660 TAP RBT071660 RG SABER 6.0 AWL-TIP LONG CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
27 00763000352066 RBT071655 TAP RBT071655 RG SABER 5.5 AWL-TIP LONG CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
28 00763000352042 RBT071645 TAP RBT071645 RG SABER 4.5 AWL-TIP LONG CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
29 00763000352035 RBT071640 TAP RBT071640 RG SABER 4.0 AWL-TIP LONG CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
30 00763000352028 RBT071575 TAP RBT071575 RG SABER 7.5 AWL-TIP SHORT CD Horizon Modulex Spinal System MEDTRONIC SOFAMOR DANEK, INC.
31 00763000352011 RBT071565 TAP RBT071565 RG SABER 6.5 AWL-TIP SHORT CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
32 00763000352004 RBT071560 TAP RBT071560 RG SABER 6.0 AWL-TIP SHORT CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
33 00763000351991 RBT071555 TAP RBT071555 RG SABER 5.5 AWL-TIP SHORT CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
34 00763000351977 RBT071545 TAP RBT071545 RG SABER 4.5 AWL-TIP SHORT CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
35 00763000351960 RBT071540 TAP RBT071540 RG SABER 4.0 AWL-TIP SHORT CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
36 00763000351953 RBT073210 DRIVER RBT073210 RG SABER SHANK 10.5 L CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
37 00763000351946 RBT076210 SLEEVE RBT076210 RG SABR SANK DRV 10.5 L CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
38 00763000351939 RBT073110 DRIVER RBT073110 RG SABER SHANK 10.5 S CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
39 00763000351922 RBT076110 SLEEVE RBT076110 RG SABR SHNK DRV 10.5 S CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
40 00763000351892 RBT074210 CANNULA RBT074210 RG SABER OUTER L 10.5 CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
41 00763000351885 RBT074110 CANNULA RBT074110 RG SABER OUTER S 10.5 CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
42 00763000340179 9732353 FRAME 9732353 PERC REF CROSS PIN N/A MEDTRONIC NAVIGATION, INC.
43 00763000340155 9731567 ASY 9731567 FIGHTER PSVE SMALL SURETRAK2 NA MEDTRONIC NAVIGATION, INC.
44 00763000255299 NAV6062116 TRIAL NAV6062116 CATALYFT PL40 NAV 11MM Catalyft PL Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
45 00763000255282 NAV6062096 TRIAL NAV6062096 CATALYFT PL40 NAV 9MM Catalyft PL Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
46 00763000255275 NAV6062076 TRIAL NAV6062076 CATALYFT PL40 NAV 7MM Catalyft PL Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
47 00763000255268 NAV6061116 TRIAL NAV6061116 CATALYFT PL NAV 11MM Catalyft PL Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
48 00763000255251 NAV6061096 TRIAL NAV6061096 CATALYFT PL NAV 9MM Catalyft PL Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
49 00763000255244 NAV6061076 TRIAL NAV6061076 CATALYFT PL NAV 7MM Catalyft PL Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.
50 00763000255237 NAV6061000 INSERTER NAV6061000 CATALYFT PL NAV Catalyft PL Expandable Interbody System MEDTRONIC SOFAMOR DANEK, INC.