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 M7408610048 86-11-23-16 861-0048 Duo Ti Angled Trial, 16mm, 15° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
2 M7408610047 86-11-23-14 861-0047 Duo Ti Angled Trial, 14mm, 15° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
3 M7408610046 86-11-23-12 861-0046 Duo Ti Angled Trial, 12mm, 15° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
4 M7408610045 86-11-22-16 861-0045 Duo Ti Angled Trial, 16mm, 8° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
5 M7408610044 86-11-22-14 861-0044 Duo Ti Angled Trial, 14mm, 8° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
6 M7408610043 86-11-22-12 861-0043 Duo Ti Angled Trial, 12mm, 8° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
7 M7408610042 86-11-22-10 861-0042 Duo Ti Angled Trial, 10mm, 8° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
8 M7408610041 86-11-21-16 861-0041 Duo Ti Angled Trial, 16mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
9 M7408610040 86-11-21-14 861-0040 Duo Ti Angled Trial, 14mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
10 M7408610039 86-11-21-12 861-0039 Duo Ti Angled Trial, 12mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
11 M7408610038 86-11-21-10 861-0038 Duo Ti Angled Trial, 10mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
12 M7408610037 86-11-21-8 861-0037 Duo Ti Angled Trial, 8mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
13 M7408610036 86-11-20-16 861-0036 Duo Ti Trial, 16mm, 15° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
14 M7408610035 86-11-20-14 861-0035 Duo Ti Trial, 14mm, 15° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
15 M7408610034 86-11-20-12 861-0034 Duo Ti Trial, 12mm, 15° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
16 M7408610033 86-11-19-16 861-0033 Duo Ti Trial, 16mm, 8° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
17 M7408610032 86-11-19-14 861-0032 Duo Ti Trial, 14mm, 8° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
18 M7408610031 86-11-19-12 861-0031 Duo Ti Trial, 12mm, 8° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
19 M7408610030 86-11-19-10 861-0030 Duo Ti Trial, 10mm, 8° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
20 M7408610029 86-11-18-16 861-0029 Duo Ti Trial, 16mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
21 M7408610028 86-11-18-14 861-0028 Duo Ti Trial, 14mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
22 M7408610027 86-11-18-12 861-0027 Duo Ti Trial, 12mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
23 M7408610026 86-11-18-10 861-0026 Duo Ti Trial, 10mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
24 M7408610025 86-11-18-8 861-0025 Duo Ti Trial, 8mm, 0° Duo Ti Expandable Interbody Fusion System SPINEOLOGY INC.
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26 M7408608110 86-08-23-2 860-8110 Duo LU Angled Trial, 14mm, 15° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
27 M7408608109 86-08-23-1 860-8109 Duo LU Angled Trial, 12mm, 15° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
28 M7408608103 86-08-21-4 860-8103 Duo LU Angled Trial, 16mm, 8° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
29 M7408608102 86-08-21-3 860-8102 Duo LU Angled Trial, 14mm, 8° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
30 M7408608101 86-08-21-2 860-8101 Duo LU Angled Trial, 12mm, 8° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
31 M7408608100 86-08-21-1 860-8100 Duo LU Angled Trial, 10mm, 8° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
32 M7408608008 86-08-17-16 860-8008 Duo Angled Trial, 16mm, 0° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
33 M7408608007 86-08-17-14 860-8007 Duo Angled Trial, 14mm, 0° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
34 M7408608006 86-08-17-12 860-8006 Duo Angled Trial, 12mm, 0° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
35 M7408608005 86-08-17-10 860-8005 Duo Angled Trial, 10mm, 0° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
36 M7408608004 86-08-17-8 860-8004 Duo Angled Trial, 8mm, 0° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
37 M7408600519 86-05-19 860-0519 Duo Angled Inserter Fork Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
38 M7408600515 86-05-15 860-0515 Duo Angled Access Inserter Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
39 M7408600514 86-05-14 860-0514 Duo Straight Inserter Fork Duo SPINEOLOGY INC.
40 M7408600501 86-05-01 860-0501 Duo Straight Inserter Duo SPINEOLOGY INC.
41 M7408600124 86-30-11-16 860-0124 Duo Trial, 16mm, 15° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
42 M7408600123 86-30-11-14 860-0123 Duo Trial, 14mm, 15° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
43 M7408600122 86-30-11-12 860-0122 Duo Trial, 12mm, 15° Duo Lumbar Interbody Fusion System SPINEOLOGY INC.
44 M7408600117 86-30-03 860-0117 Duo Trial Inserter Duo SPINEOLOGY INC.
45 M7408600109 86-30-10-16 860-0109 Duo Trial, 16mm, 8° Duo SPINEOLOGY INC.
46 M7408600108 86-30-10-14 860-0108 Duo Trial, 14mm, 8° Duo SPINEOLOGY INC.
47 M7408600107 86-30-10-12 860-0107 Duo Trial, 12mm, 8° Duo SPINEOLOGY INC.
48 M7408600106 86-30-10-10 860-0106 Duo Trial, 10mm, 8° Duo SPINEOLOGY INC.
49 M7408600105 86-30-09-16 860-0105 Duo Trial, 16mm NL Duo SPINEOLOGY INC.
50 M7408600104 86-30-09-14 860-0104 Duo Trial, 14mm NL Duo SPINEOLOGY INC.