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 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 "LRP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00191375052647 1370-030-001 1370-030-001 Rigid Tray System, Instruments Set 1.5 ENDOSKELETON® TL TITAN SPINE, LLC
2 00191375052630 1372-030-002 1372-030-002 Rigid Tray System, Instruments Set 3.5 ENDOSKELETON® TL TITAN SPINE, LLC
3 00191375052623 1372-030-001 1372-030-001 Rigid Tray System, Instruments Set 3.5 ENDOSKELETON® TL TITAN SPINE, LLC
4 00191375052616 1374-030-002 1374-030-002 Rigid Tray System, Instruments Set 5.5 ENDOSKELETON® TL TITAN SPINE, LLC
5 00191375052869 11-04414-00 TRAY 11-04414-00 TAS PERFORATED TRAY Endoskeleton™ TAS Interbody System MEDTRONIC SOFAMOR DANEK, INC.
6 00191375052852 1156-040-212 Anterolateral Implant Caddy ENDOSKELETON® TAS MEDTRONIC SOFAMOR DANEK, INC.
7 00191375052845 3340-0126 3340-0126 Perforated Tray, Lid ENDOSKELETON® TA TITAN SPINE, LLC
8 00191375052838 3050-2131 3050-2131 Perforated Tray, Base ENDOSKELETON® TA TITAN SPINE, LLC
9 00191375052821 3051-2087 Instrument Case - Mid Tray ENDOSKELETON® TC MEDTRONIC SOFAMOR DANEK, INC.
10 00191375052814 3051-2088 Instrument Case - Base ENDOSKELETON® TC MEDTRONIC SOFAMOR DANEK, INC.
11 00191375052807 3051-0150 TLIF Case Tray ENDOSKELETON® TT MEDTRONIC SOFAMOR DANEK, INC.
12 00191375052791 3341-0019 TLIF Case Lid ENDOSKELETON® TT MEDTRONIC SOFAMOR DANEK, INC.
13 00191375052784 3051-0151 TLIF Case Tray ENDOSKELETON® TT MEDTRONIC SOFAMOR DANEK, INC.
14 00191375052777 3051-0149 TLIF Case Base ENDOSKELETON® TT MEDTRONIC SOFAMOR DANEK, INC.
15 00191375052760 1379-030-001 1379-030-001 Plate Instrument, Perforated Tray, Base ENDOSKELETON® TAS TITAN SPINE, LLC
16 00191375052753 1378-030-001 Plate Instrument Set 1.1 ENDOSKELETON® TCS MEDTRONIC SOFAMOR DANEK, INC.
17 00191375052586 1376-030-001 1376-030-001 Rigid Tray System, Angled Instruments Set 2.3 ENDOSKELETON® TL TITAN SPINE, LLC
18 00191375052579 1284-010-001 Generic Lid ENDOSKELETON® MEDTRONIC SOFAMOR DANEK, INC.
19 00191375052562 1377-030-001 1377-030-001 Rigid Tray System, Angled Instruments Set 3.3 ENDOSKELETON® TL TITAN SPINE, LLC
20 00191375052555 1377-030-002 1377-030-002 Rigid Tray System, Angled Instruments Set 3.3 ENDOSKELETON® TL TITAN SPINE, LLC
21 00191375052418 2200-0001-20 Impant Caddy, Lid ENDOSKELETON® TA VBR MEDTRONIC SOFAMOR DANEK, INC.
22 00191375052340 TS-6000-04-2 Quick Inserter Attachment Caddy, Lid ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
23 00191375052333 TS-6000-04-1 Quick Inserter Attachment Caddy, Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
24 00191375052326 TS-6000-03 Perforated, Instrument Tray, Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
25 00191375052319 TS-5000-02 Perforated, Upper, Inner Tray, Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
26 00191375052302 TS-5000-01 Perforated, Lower, Inner Tray, Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
27 00191375052296 TS-4000-07-2 40mm, Caddy, Lid ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
28 00191375052289 TS-4000-07-1 40mm, Caddy, Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
29 00191375052272 TS-4000-06 Perforated, Instrument Tray, Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
30 00191375052265 TS-4000-05-2 7 Deg Lordotic, Rasp Caddy, Lid ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
31 00191375052258 TS-4000-05-1 7 Deg Lordotic, Rasp Caddy, Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
32 00191375052241 TS-4000-04-2 7 Deg Lordotic, Trials Caddy, Lid ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
33 00191375052234 TS-4000-04-1 7 Deg Lordotic, Trials Caddy, Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
34 00191375052227 TS-4000-03 Perforated, Tray, Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
35 00191375052210 TS-4000-02-2 7 Deg Lordotic, Implant, Caddy, Lid, 22mm ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
36 00191375052203 TS-4000-02-1 7 Deg Lordotic, Implant, Caddy, Base, 22mm ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
37 00191375052180 TS-4000-01-2 7 Deg Lordotic, Implant, Caddy, Lid, 18mm ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
38 00191375052173 TS-4000-01-1 7 Deg Lordotic, Implant, Caddy, Base, 18mm ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
39 00191375052159 TS-2000-04 Perforated, Instrument Tray Base ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
40 00191375052142 TS-2000-03 Perforated, Tray, Lid ENDOSKELETON® TL MEDTRONIC SOFAMOR DANEK, INC.
41 00191375052111 920-042-002 Caddy, Base ENDOSKELETON® TO MEDTRONIC SOFAMOR DANEK, INC.
42 00191375052104 920-041-001 Caddy, Lid ENDOSKELETON® TO MEDTRONIC SOFAMOR DANEK, INC.
43 00191375052098 920-020-001 Perforated, Tray, Base ENDOSKELETON® TO MEDTRONIC SOFAMOR DANEK, INC.
44 00191375052074 900-020-001 Expandable Distractor, Perforated, Tray, Base ENDOSKELETON® TT MEDTRONIC SOFAMOR DANEK, INC.
45 00191375052067 863-020-001 Perforated, Tray, Base ENDOSKELETON® TO MEDTRONIC SOFAMOR DANEK, INC.
46 00191375052050 859-020-001 Articulating Inserter, Perforated Tray, Base ENDOSKELETON® TT MEDTRONIC SOFAMOR DANEK, INC.
47 00191375052012 830-020-001 Quick Inserter, Perforated, Tray, Base ENDOSKELETON® TAS MEDTRONIC SOFAMOR DANEK, INC.
48 00191375051954 687-030-101 Anterolateral Perforated, Inner Tray ENDOSKELETON® TAS MEDTRONIC SOFAMOR DANEK, INC.
49 00191375051947 687-020-001 Anterolateral Perforated, Tray, Base ENDOSKELETON® TAS MEDTRONIC SOFAMOR DANEK, INC.
50 00191375051893 588-020-001 Perforated, Tray, Base ENDOSKELETON® TO MEDTRONIC SOFAMOR DANEK, INC.