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 "MAX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00613994916341 X0910108 SPACER X0910108 PER TI LG 8D 30X12 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
2 00613994916334 X0910109 SPACER X0910109 PER TI LG 8D 30X14 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
3 00613994916327 X0910110 SPACER X0910110 PER TI LG 8D 30X16 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
4 00613994916310 X0910111 SPACER X0910111 PER TI LG 8D 30X18 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
5 00613994916303 X0910112 SPACER X0910112 PER TI LG 8D 30X20 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
6 00613994916297 X0910113 SPACER X0910113 PER TI LG 12D 30X8 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
7 00613994916280 X0910114 SPACER X0910114 PER TI LG 12D 30X10 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
8 00613994916273 X0910115 SPACER X0910115 PER TI LG 12D 30X12 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
9 00613994916266 X0910116 SPACER X0910116 PER TI LG 12D 30X14 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
10 00613994916259 X0910117 SPACER X0910117 PER TI LG 12D 30X16 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
11 00613994916242 X0910118 SPACER X0910118 PER TI LG 12D 30X18 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
12 00613994916235 X0910119 SPACER X0910119 PER TI LG 12D 30X20 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
13 00613994916228 X0910120 SPACER X0910120 PER TI XL 8D 36X8 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
14 00613994916211 X0910121 SPACER X0910121 PER TI XL 8D 36X10 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
15 00613994916204 X0910122 SPACER X0910122 PER TI XL 8D 36X12 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
16 00613994916198 X0910107 SPACER X0910107 PER TI LG 8D 30X10 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
17 00613994916181 X0910092 SPACER X0910092 PER TI MD 8D 26X8 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
18 00613994916174 X0910093 SPACER X0910093 PER TI MD 8D 26X10 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
19 00613994916167 X0910094 SPACER X0910094 PER TI MD 8D 26X12 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
20 00613994916150 X0910095 SPACER X0910095 PER TI MD 8D 26X14 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
21 00613994916143 X0910096 SPACER X0910096 PER TI MD 8D 26X16 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
22 00613994916136 X0910097 SPACER X0910097 PER TI MD 8D 26X18 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
23 00613994916129 X0910098 SPACER X0910098 PER TI MD 8D 26X20 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
24 00613994916112 X0910099 SPACER X0910099 PER TI MD 12D 26X8 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
25 00613994916105 X0910100 SPACER X0910100 PER TI MD 12D 26X10 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
26 00613994916099 X0910101 SPACER X0910101 PER TI MD 12D 26X12 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
27 00613994916082 X0910102 SPACER X0910102 PER TI MD 12D 26X14 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
28 00613994916075 X0910103 SPACER X0910103 PER TI MD 12D 26X16 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
29 00613994916068 X0910104 SPACER X0910104 PER TI MD 12D 26X18 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
30 00613994916051 X0910105 SPACER X0910105 PER TI MD 12D 26X20 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
31 00613994916044 X0910106 SPACER X0910106 PER TI LG 8D 30X8 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
32 00613994916037 X1110073 SPACER X1110073 PER TI XXL 8D 38X18 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
33 00613994916020 X1110074 SPACER X1110074 PER TI XXL 8D 38X20 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
34 00613994916013 X1110075 SPACER X1110075 PER TI XXL 12D 38X8 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
35 00613994916006 X1110076 SPACER X1110076 PER TI XXL 12D 38X10 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
36 00613994915993 X1110077 SPACER X1110077 PER TI XXL 12D 38X12 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
37 00613994915986 X1110078 SPACER X1110078 PER TI XXL 12D 38X14 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
38 00613994915979 X1110079 SPACER X1110079 PER TI XXL 12D 38X16 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
39 00613994915962 X1110080 SPACER X1110080 PER TI XXL 12D 38X18 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
40 00613994915955 X1110081 SPACER X1110081 PER TI XXL 12D 38X20 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
41 00613994915948 X1110083 SPACER X1110083 PER TI XXL 15D 38X10 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
42 00613994915931 X1110084 SPACER X1110084 PER TI XXL 15D 38X12 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
43 00613994915924 X1110085 SPACER X1110085 PER TI XXL 15D 38X14 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
44 00613994915917 X1110086 SPACER X1110086 PER TI XXL 15D 38X16 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
45 00613994915900 X1110087 SPACER X1110087 PER TI XXL 15D 38X18 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
46 00613994915894 X1110088 SPACER X1110088 PER TI XXL 15D 38X20 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
47 00613994915887 X1110072 SPACER X1110072 PER TI XXL 8D 38X16 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
48 00613994915870 X0910123 SPACER X0910123 PER TI XL 8D 36X14 PERIMETER® Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
49 00613994915863 X0910124 SPACER X0910124 PER TI XL 8D 36X16 Perimeter Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.
50 00613994915856 X0910125 SPACER X0910125 PER TI XL 8D 36X18 Perimeter Interbody Fusion Device MEDTRONIC SOFAMOR DANEK, INC.