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 10845854017173 BXS6220 BXS6220 1.5MM BONE FIXATION KIT, DIAMETER 1.5 X 20MM, QTY 2 NA CONMED CORPORATION
2 10845854017170 BXS6220 BXS6220 1.5MM BONE FIXATION KIT, DIAMETER 1.5 X 20MM, QTY 2 NA CONMED CORPORATION
3 10845854017166 BXS6216 BXS6216 1.5MM BONE FIXATION KIT, DIAMETER 1.5 X 16MM, QTY 2 NA CONMED CORPORATION
4 10845854017163 BXS6216 BXS6216 1.5MM BONE FIXATION KIT, DIAMETER 1.5 X 16MM, QTY 2 NA CONMED CORPORATION
5 10845854017159 BXS6225 BXS6225 1.5MM BONE FIXATION KIT, DIAMETER 1.5 X 25MM, QTY 2 NA CONMED CORPORATION
6 10845854017156 BXS6225 BXS6225 1.5MM BONE FIXATION KIT, DIAMETER 1.5 X 25MM, QTY 2 NA CONMED CORPORATION
7 10845854017135 231025M5 231025M5 GENESYS MATRYX 10.0 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
8 10845854017132 231025M5 231025M5 GENESYS MATRYX 10.0 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
9 10845854017128 238035M5 238035M5 GENESYS MATRYX 8.0 X 35 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
10 10845854017125 238035M5 238035M5 GENESYS MATRYX 8.0 X 35 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
11 10845854017118 236520M5 236520M5 GENESYS MATRYX 6.5 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
12 10845854017111 236520M5 236520M5 GENESYS MATRYX 6.5 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
13 10845854017098 236025M5 236025M5 GENESYS MATRYX 6.0 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
14 10845854017095 236025M5 236025M5 GENESYS MATRYX 6.0 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
15 10845854017088 231125M5 231125M5 GENESYS MATRYX 11.0 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
16 10845854017081 231125M5 231125M5 GENESYS MATRYX 11.0 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
17 10845854017074 235030M5 235030M5 GENESYS MATRYX 5.0 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
18 10845854017071 235030M5 235030M5 GENESYS MATRYX 5.0 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
19 10845854017067 231020M5 231020M5 GENESYS MATRYX 10.0 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
20 10845854017064 231020M5 231020M5 GENESYS MATRYX 10.0 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
21 10845854017057 237025M5 237025M5 GENESYS MATRYX 7.0 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
22 10845854017050 237025M5 237025M5 GENESYS MATRYX 7.0 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
23 10845854017043 236515M5 236515M5 GENESYS MATRYX 6.5 X 15 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
24 10845854017040 236515M5 236515M5 GENESYS MATRYX 6.5 X 15 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
25 10845854017036 231030M5 231030M5 GENESYS MATRYX 10.0 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
26 10845854017033 231030M5 231030M5 GENESYS MATRYX 10.0 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
27 10845854017029 231120M5 231120M5 GENESYS MATRYX 11.0 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
28 10845854017026 231120M5 231120M5 GENESYS MATRYX 11.0 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
29 10845854017005 239035M5 239035M5 GENESYS MATRYX 9.0 X 35 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
30 10845854017002 239035M5 239035M5 GENESYS MATRYX 9.0 X 35 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
31 10845854016999 235525M5 235525M5 GENESYS MATRYX 5.5 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
32 10845854016992 235525M5 235525M5 GENESYS MATRYX 5.5 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
33 10845854016985 236020M5 236020M5 GENESYS MATRYX 6.0 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
34 10845854016982 236020M5 236020M5 GENESYS MATRYX 6.0 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
35 10845854016978 231135M5 231135M5 GENESYS MATRYX 11.0 X 35 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
36 10845854016975 231135M5 231135M5 GENESYS MATRYX 11.0 X 35 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
37 10845854016968 237030M5 237030M5 GENESYS MATRYX 7.0 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
38 10845854016961 237030M5 237030M5 GENESYS MATRYX 7.0 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
39 10845854016954 238030M5 238030M5 GENESYS MATRYX 8.0 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
40 10845854016951 238030M5 238030M5 GENESYS MATRYX 8.0 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
41 10845854016947 235520M5 235520M5 GENESYS MATRYX 5.5 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
42 10845854016944 235520M5 235520M5 GENESYS MATRYX 5.5 X 20 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
43 10845854016937 236530M5 236530M5 GENESYS MATRYX 6.5 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
44 10845854016930 236530M5 236530M5 GENESYS MATRYX 6.5 X 30 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
45 10845854016916 235515M5 235515M5 GENESYS MATRYX 5.5 X 15 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
46 10845854016913 235515M5 235515M5 GENESYS MATRYX 5.5 X 15 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
47 10845854016909 236525M5 236525M5 GENESYS MATRYX 6.5 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
48 10845854016906 236525M5 236525M5 GENESYS MATRYX 6.5 X 25 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
49 10845854016893 231035M5 231035M5 GENESYS MATRYX 10.0 X 35 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION
50 10845854016890 231035M5 231035M5 GENESYS MATRYX 10.0 X 35 MM INTERFERENCE SCREW GENESYS MATRYX CONMED CORPORATION