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 "HWC"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 07613327095197 619920S 619920S Washer VARIAX STRYKER TRAUMA SA
2 07613327095180 390016 390016 Washer NA STRYKER TRAUMA SA
3 07613327095173 619920 619920 Washer VARIAX STRYKER TRAUMA SA
4 07613327095166 390017 390017 Washer NA STRYKER TRAUMA SA
5 07613327095128 940180 940180 Upper Tray Foot & Ankle FIXOS STRYKER TRAUMA SA
6 07613327095111 705235S 705235S Unthreaded Guide Wire FIXOS STRYKER TRAUMA SA
7 07613327095081 705234S 705234S Unthreaded Guide Wire FIXOS STRYKER TRAUMA SA
8 07613327095074 705233S 705233S Unthreaded Guide Wire FIXOS STRYKER TRAUMA SA
9 07613327093964 627738S 627738S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
10 07613327093957 627738 627738 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
11 07613327093940 627736S 627736S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
12 07613327093933 627736 627736 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
13 07613327093926 627735S 627735S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
14 07613327093919 627735 627735 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
15 07613327093896 627734S 627734S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
16 07613327093889 627734 627734 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
17 07613327093872 627752S 627752S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
18 07613327093865 627750S 627750S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
19 07613327093858 627748S 627748S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
20 07613327093841 627746S 627746S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
21 07613327093827 627744 627744 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
22 07613327093810 627744S 627744S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
23 07613327093797 627742S 627742S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
24 07613327093780 627742 627742 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
25 07613327093773 627740S 627740S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
26 07613327093766 627740 627740 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
27 07613327093742 627708S 627708S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
28 07613327093735 627706S 627706S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
29 07613327093728 627708 627708 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
30 07613327093704 627706 627706 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
31 07613327093698 627705S 627705S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
32 07613327093681 627705 627705 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
33 07613327093674 627704 627704 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
34 07613327093667 627704S 627704S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
35 07613327093650 627720S 627720S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
36 07613327093643 627718S 627718S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
37 07613327093636 627722S 627722S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
38 07613327093629 627716S 627716S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
39 07613327093605 627714 627714 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
40 07613327093599 627714S 627714S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
41 07613327093568 627712S 627712S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
42 07613327093551 627712 627712 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
43 07613327093544 627710S 627710S Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
44 07613327093537 627710 627710 Tibial Plate; proximal medial AXSOS STRYKER TRAUMA SA
45 07613327093513 705236S 705236S Threaded Guide Wire FIXOS STRYKER TRAUMA SA
46 07613327092257 940202 940202 Silicon Mat VARIAX STRYKER TRAUMA SA
47 07613327091724 940190 940190 Screw-Rack 7.0 mm FIXOS STRYKER TRAUMA SA
48 07613327091625 940085 940085 Screw Rack T10 3.5/2.7mm VARIAX STRYKER TRAUMA SA
49 07613327091618 940201 940201 Screw Rack Lid VARIAX STRYKER TRAUMA SA
50 07613327091342 627238 627238 Proximal Lateral Humerus Plate, RIGHT AXSOS STRYKER TRAUMA SA