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 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 07630040728270 03.27.158 Posterior Interbody Fusion Device PEEK/Ti 9x25x15 L20° MectaLIF MEDACTA INTERNATIONAL SA
2 07630040728263 03.27.157 Posterior Interbody Fusion Device PEEK/Ti 9x25x15 L15° MectaLIF MEDACTA INTERNATIONAL SA
3 07630040728256 03.27.156 Posterior Interbody Fusion Device PEEK/Ti 9x25x14 L15° MectaLIF MEDACTA INTERNATIONAL SA
4 07630040728249 03.27.155 Posterior Interbody Fusion Device PEEK/Ti 9x22x15 L20° MectaLIF MEDACTA INTERNATIONAL SA
5 07630040728232 03.27.154 Posterior Interbody Fusion Device PEEK/Ti 9x22x14 L20° MectaLIF MEDACTA INTERNATIONAL SA
6 07630040728225 03.27.153 Posterior Interbody Fusion Device PEEK/Ti 9x22x15 L15° MectaLIF MEDACTA INTERNATIONAL SA
7 07630040728218 03.27.152 Posterior Interbody Fusion Device PEEK/Ti 9x22x14 L15° MectaLIF MEDACTA INTERNATIONAL SA
8 07630040728201 03.27.151 Posterior Interbody Fusion Device PEEK/Ti 9x22x13 L15° MectaLIF MEDACTA INTERNATIONAL SA
9 07630040728195 03.21.158 Posterior Interbody Fusion Device 9x25x15 L20° MectaLIF MEDACTA INTERNATIONAL SA
10 07630040728188 03.21.157 Posterior Interbody Fusion Device 9x25x15 L15° MectaLIF MEDACTA INTERNATIONAL SA
11 07630040728171 03.21.156 Posterior Interbody Fusion Device 9x25x14 L15° MectaLIF MEDACTA INTERNATIONAL SA
12 07630040728164 03.21.155 Posterior Interbody Fusion Device 9x22x15 L20° MectaLIF MEDACTA INTERNATIONAL SA
13 07630040728157 03.21.154 Posterior Interbody Fusion Device 9x22x14 L20° MectaLIF MEDACTA INTERNATIONAL SA
14 07630040728140 03.21.153 Posterior Interbody Fusion Device 9x22x15 L15° MectaLIF MEDACTA INTERNATIONAL SA
15 07630040728133 03.21.152 Posterior Interbody Fusion Device 9x22x14 L15° MectaLIF MEDACTA INTERNATIONAL SA
16 07630040728126 03.21.151 Posterior Interbody Fusion Device 9x22x13 L15° MectaLIF MEDACTA INTERNATIONAL SA
17 07630040719803 03.27.150 Posterior Interbody Fusion Device PEEK/Ti 9x25x15 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
18 07630040719797 03.27.149 Posterior Interbody Fusion Device PEEK/Ti 9x25x14 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
19 07630040719780 03.27.148 Posterior Interbody Fusion Device PEEK/Ti 9x25x13 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
20 07630040719773 03.27.147 Posterior Interbody Fusion Device PEEK/Ti 9x25x12 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
21 07630040719766 03.27.146 Posterior Interbody Fusion Device PEEK/Ti 9x25x11 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
22 07630040719759 03.27.145 Posterior Interbody Fusion Device PEEK/Ti 9x25x10 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
23 07630040719742 03.27.144 Posterior Interbody Fusion Device PEEK/Ti 9x25x9 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
24 07630040719735 03.27.143 Posterior Interbody Fusion Device PEEK/Ti 9x25x15 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
25 07630040719728 03.27.142 Posterior Interbody Fusion Device PEEK/Ti 9x25x14 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
26 07630040719711 03.27.141 Posterior Interbody Fusion Device PEEK/Ti 9x25x13 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
27 07630040719704 03.27.140 Posterior Interbody Fusion Device PEEK/Ti 9x25x12 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
28 07630040719698 03.27.139 Posterior Interbody Fusion Device PEEK/Ti 9x25x11 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
29 07630040719681 03.27.138 Posterior Interbody Fusion Device PEEK/Ti 9x25x10 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
30 07630040719674 03.27.137 Posterior Interbody Fusion Device PEEK/Ti 9x25x9 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
31 07630040719667 03.27.136 Posterior Interbody Fusion Device PEEK/Ti 9x25x8 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
32 07630040719650 03.27.135 Posterior Interbody Fusion Device PEEK/Ti 9x25x7 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
33 07630040719643 03.27.134 Posterior Interbody Fusion Device PEEK/Ti 9x25x15 L0° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
34 07630040719636 03.27.133 Posterior Interbody Fusion Device PEEK/Ti 9x25x14 L0° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
35 07630040719629 03.27.132 Posterior Interbody Fusion Device PEEK/Ti 9x25x13 L0° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
36 07630040719612 03.27.131 Posterior Interbody Fusion Device PEEK/Ti 9x25x12 L0° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
37 07630040719605 03.27.130 Posterior Interbody Fusion Device PEEK/Ti 9x25x11 L0° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
38 07630040719599 03.27.129 Posterior Interbody Fusion Device PEEK/Ti 9x25x10 L0° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
39 07630040719582 03.27.128 Posterior Interbody Fusion Device PEEK/Ti 9x25x9 L0° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
40 07630040719575 03.27.127 Posterior Interbody Fusion Device PEEK/Ti 9x25x8 L0° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
41 07630040719568 03.27.126 Posterior Interbody Fusion Device PEEK/Ti 9x25x7 L0° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
42 07630040719551 03.27.125 Posterior Interbody Fusion Device PEEK/Ti 9x22x15 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
43 07630040719544 03.27.124 Posterior Interbody Fusion Device PEEK/Ti 9x22x14 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
44 07630040719537 03.27.123 Posterior Interbody Fusion Device PEEK/Ti 9x22x13 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
45 07630040719520 03.27.122 Posterior Interbody Fusion Device PEEK/Ti 9x22x12 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
46 07630040719513 03.27.121 Posterior Interbody Fusion Device PEEK/Ti 9x22x11 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
47 07630040719506 03.27.120 Posterior Interbody Fusion Device PEEK/Ti 9x22x10 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
48 07630040719490 03.27.119 Posterior Interbody Fusion Device PEEK/Ti 9x22x9 L10° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
49 07630040719483 03.27.118 Posterior Interbody Fusion Device PEEK/Ti 9x22x15 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA
50 07630040719476 03.27.117 Posterior Interbody Fusion Device PEEK/Ti 9x22x14 L5° Mectalif Posterior Cages MEDACTA INTERNATIONAL SA