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 90814008024868 PLE-609-M PLIF Encoded 10x26 9mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
13 90814008024851 PLE-608-M PLIF Encoded 10x26 8mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
14 90814008024844 PLE-607-M PLIF Encoded 10x26 7mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
15 90814008024837 PLE-015-M PLIF Encoded 10x26 15mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
16 90814008024820 PLE-014-M PLIF Encoded 10x26 14mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
17 90814008024813 PLE-013-M PLIF Encoded 10x26 13mm 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 10889910058434 33-2007 33-2007 Pacifica-S Implant, 9mm x 20mm x 7mm SeaSpine Spacer System - Pacifica™ SEASPINE ORTHOPEDICS CORPORATION
2 10888857556041 PRO-1255-16 PRO-1255-16 Cervical Disc Trial Size 13x16x12 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
3 10888857556034 PRO-1255-15 PRO-1255-15 Cervical Disc Trial Size 13x16x11 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
4 10888857556027 PRO-1255-14 PRO-1255-14 Cervical Disc Trial Size 13x16x10 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
5 10888857556010 PRO-1255-13 PRO-1255-13 Cervical Disc Trial Size 13x16x9 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
6 10888857556003 PRO-1255-12 PRO-1255-12 Cervical Disc Trial Size 13x16x8 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
7 10888857555990 PRO-1255-11 PRO-1255-11 Cervical Disc Trial Size 13x16x7 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
8 10888857555983 PRO-1255-10 PRO-1255-10 Cervical Disc Trial Size 13x16x6 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
9 10888857555976 PRO-1255-09 PRO-1255-09 Cervical Disc Trial Size 13x16x5 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
10 10888857555969 PRO-1255-08 PRO-1255-08 Cervical Disc Trial Size 12x14x12 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
11 10888857555952 PRO-1255-07 PRO-1255-07 Cervical Disc Trial Size 12x14x11 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
12 10888857555945 PRO-1255-06 PRO-1255-06 Cervical Disc Trial Size 12x14x10 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
13 10888857555938 PRO-1255-05 PRO-1255-05 Cervical Disc Trial Size 12x14x9 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
14 10888857555921 PRO-1255-04 PRO-1255-04 Cervical Disc Trial Size 12x14x8 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
15 10888857555914 PRO-1255-03 PRO-1255-03 Cervical Disc Trial Size 12x14x7 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
16 10888857555907 PRO-1255-02 PRO-1255-02 Cervical Disc Trial Size 12x14x6 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
17 10888857555891 PRO-1255-01 PRO-1255-01 Cervical Disc Trial Size 12x14x5 mm, 7° ALEUTIAN Interbody Systems K2M, INC.
18 10888857554740 PRO-1238-20 PRO-1238-20 Trial Size 16x20x15 mm, Convex CASCADIA™ Interbody System K2M, INC.
19 10888857554733 PRO-1238-19 PRO-1238-19 Trial Size 16x20x14 mm, Convex CASCADIA™ Interbody System K2M, INC.
20 10888857554726 PRO-1238-18 PRO-1238-18 Trial Size 16x20x13 mm, Convex CASCADIA™ Interbody System K2M, INC.
21 10888857554719 PRO-1238-17 PRO-1238-17 Trial Size 16x20x12 mm, Convex CASCADIA™ Interbody System K2M, INC.
22 10888857554702 PRO-1238-16 PRO-1238-16 Trial Size 16x20x11 mm, Convex CASCADIA™ Interbody System K2M, INC.
23 10888857554696 PRO-1238-15 PRO-1238-15 Trial Size 16x20x10 mm, Convex CASCADIA™ Interbody System K2M, INC.
24 10888857554689 PRO-1238-14 PRO-1238-14 Trial Size 16x20x9 mm, Convex CASCADIA™ Interbody System K2M, INC.
25 10888857554672 PRO-1238-13 PRO-1238-13 Trial Size 16x20x8 mm, Convex CASCADIA™ Interbody System K2M, INC.
26 10888857554665 PRO-1238-12 PRO-1238-12 Trial Size 16x20x7 mm, Convex CASCADIA™ Interbody System K2M, INC.
27 10888857554658 PRO-1238-11 PRO-1238-11 Trial Size 16x20x6 mm, Convex CASCADIA™ Interbody System K2M, INC.
28 10888857554641 PRO-1238-10 PRO-1238-10 Trial Size 14x18x15 mm, Convex CASCADIA™ Interbody System K2M, INC.
29 10888857554634 PRO-1238-09 PRO-1238-09 Trial Size 14x18x14 mm, Convex CASCADIA™ Interbody System K2M, INC.
30 10888857554627 PRO-1238-08 PRO-1238-08 Trial Size 14x18x13 mm, Convex CASCADIA™ Interbody System K2M, INC.
31 10888857554610 PRO-1238-07 PRO-1238-07 Trial Size 14x18x12 mm, Convex CASCADIA™ Interbody System K2M, INC.
32 10888857554603 PRO-1238-06 PRO-1238-06 Trial Size 14x18x11 mm, Convex CASCADIA™ Interbody System K2M, INC.
33 10888857554597 PRO-1238-05 PRO-1238-05 Trial Size 14x18x10 mm, Convex CASCADIA™ Interbody System K2M, INC.
34 10888857554580 PRO-1238-04 PRO-1238-04 Trial Size 14x18x9 mm, Convex CASCADIA™ Interbody System K2M, INC.
35 10888857554573 PRO-1238-03 PRO-1238-03 Trial Size 14x18x8 mm, Convex CASCADIA™ Interbody System K2M, INC.
36 10888857554566 PRO-1238-02 PRO-1238-02 Trial Size 14x18x7 mm, Convex CASCADIA™ Interbody System K2M, INC.
37 10888857554559 PRO-1238-01 PRO-1238-01 Trial Size 14x18x6 mm, Convex CASCADIA™ Interbody System K2M, INC.
38 10888857549159 PRO-1167-02 PRO-1167-02 Inserter Inner Shaft ALEUTIAN® Interbody Systems K2M, INC.
39 10888857549142 PRO-1167-01 PRO-1167-01 Adjustable Inserter ALEUTIAN® Interbody Systems K2M, INC.
40 10888857548794 PRO-1165-02 PRO-1165-02 Inner Shaft CASCADIA™ Interbody System K2M, INC.
41 10888857548763 PRO-1161-01 PRO-1161-01 Trial Inserter ALEUTIAN® Interbody Systems K2M, INC.
42 10888857528260 PRO-1109 PRO-1109 Trial Inserter Size 25° ALEUTIAN® Interbody Systems K2M, INC.
43 10888857525061 PRO-1093-11 PRO-1093-11 Trial With Stop Size 12x14x15 mm, 7° ALEUTIAN® Interbody Systems K2M, INC.
44 10888857525054 PRO-1093-10 PRO-1093-10 Trial With Stop Size 12x14x14 mm, 7° ALEUTIAN® Interbody Systems K2M, INC.
45 10888857525047 PRO-1093-09 PRO-1093-09 Trial With Stop Size 12x14x13 mm, 7° ALEUTIAN® Interbody Systems K2M, INC.
46 10888857525030 PRO-1093-08 PRO-1093-08 Trial With Stop Size12x14x12 mm, 7° ALEUTIAN® Interbody Systems K2M, INC.
47 10888857525023 PRO-1093-07 PRO-1093-07 Trial With Stop Size 12x14x11 mm, 7° ALEUTIAN® Interbody Systems K2M, INC.
48 10888857525016 PRO-1093-06 PRO-1093-06 Trial With Stop Szie 12x14x10 mm, 7° ALEUTIAN® Interbody Systems K2M, INC.
49 10888857525009 PRO-1093-05 PRO-1093-05 Trial With Stop Size12x14x9 mm, 7° ALEUTIAN® Interbody Systems K2M, INC.
50 10888857524996 PRO-1093-04 PRO-1093-04 Trial With Stop Size 12x14x8 mm, 7° ALEUTIAN® Interbody Systems K2M, INC.