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 00857915007569 6300-11-35 Secure Screw 35mm Secure Screw 35mm A.M. SURGICAL, INC.
2 00857915007262 6300-K Secure Screw Starter Pack Secure Screw Starter Pack A.M. SURGICAL, INC.
3 00857915007231 6300-11-60 Secure Screw 60mm Secure Screw 60mm A.M. SURGICAL, INC.
4 00857915007224 6300-11-55 Secure Screw 55mm Secure Screw 55mm A.M. SURGICAL, INC.
5 00857915007217 6300-11-50 Secure Screw 50mm Secure Screw 50mm A.M. SURGICAL, INC.
6 00857915007200 6300-11-45 Secure Screw 45mm Secure Screw 45mm A.M. SURGICAL, INC.
7 00857915007194 6300-11-40 Secure Screw 40mm Secure Screw 40mm A.M. SURGICAL, INC.
8 00854865007595 323.1033 323.1033 AdvantageRib Short Bridge and 23mm Locking Posts AdvantageRib SIG MEDICAL CORP.
9 00854865007588 323.1032 323.1032 AdvantageRib Short Bridge and 18mm Locking Posts AdvantageRib SIG MEDICAL CORP.
10 00854865007571 323.1031 323.1031 AdvantageRib Short Bridge and 11mm Locking Posts AdvantageRib SIG MEDICAL CORP.
11 00854865007564 323.1030 323.1030 AdvantageRib Short Bridge and 10mm Locking Posts AdvantageRib SIG MEDICAL CORP.
12 00854865007557 323.1023 323.1023 AdvantageRib Short Bridge and 23mm Locking Posts AdvantageRib SIG MEDICAL CORP.
13 00854865007540 323.1022 323.1022 AdvantageRib Short Bridge and 18mm Locking Posts AdvantageRib SIG MEDICAL CORP.
14 00854865007533 323.1021 323.1021 AdvantageRib Short Bridge and 11mm Locking Posts AdvantageRib SIG MEDICAL CORP.
15 00854865007526 323.1020 323.1020 AdvantageRib Short Bridge and 10mm Locking Posts AdvantageRib SIG MEDICAL CORP.
16 00854865007519 323.1013 323.1013 AdvantageRib Short Bridge and 23mm Locking Posts AdvantageRib SIG MEDICAL CORP.
17 00854865007502 323.1012 323.1012 AdvantageRib Short Bridge and 18mm Locking Posts AdvantageRib SIG MEDICAL CORP.
18 00854865007496 323.1011 323.1011 AdvantageRib Short Bridge and 11mm Locking Posts AdvantageRib SIG MEDICAL CORP.
19 00854865007489 323.1010 323.1010 AdvantageRib Short Bridge and 10mm Locking Posts AdvantageRib SIG MEDICAL CORP.
20 00853785008576 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 60 22761-0021-2.7-60 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 60 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
21 00853785008569 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 58 22761-0021-2.7-58 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 58 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
22 00853785008552 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 56 22761-0021-2.7-56 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 56 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
23 00853785008545 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 54 22761-0021-2.7-54 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 54 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
24 00853785008538 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 52 22761-0021-2.7-52 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 52 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
25 00853785008521 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 50 22761-0021-2.7-50 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 50 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
26 00853785008514 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 48 22761-0021-2.7-48 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 48 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
27 00853785008507 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 46 22761-0021-2.7-46 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 46 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
28 00853785008491 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 44 22761-0021-2.7-44 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 44 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
29 00853785008484 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 42 22761-0021-2.7-42 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 42 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
30 00853785008477 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 40 22761-0021-2.7-40 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 40 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
31 00853785008460 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 38 22761-0021-2.7-38 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 38 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
32 00853785008453 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 36 22761-0021-2.7-36 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 36 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
33 00853785008446 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 34 22761-0021-2.7-34 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 34 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
34 00853785008439 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 32 22761-0021-2.7-32 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 32 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
35 00853785008422 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 30 22761-0021-2.7-30 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 30 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
36 00853785008415 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 28 22761-0021-2.7-28 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 28 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
37 00853785008408 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 26 22761-0021-2.7-26 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 26 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
38 00853785008392 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 24 22761-0021-2.7-24 4.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 24 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
39 00853785008385 3.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 44 22761-0020-2.7-44 3.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 44 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
40 00853785008378 3.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 42 22761-0020-2.7-42 3.0MM CANNULATED SCREW, SQUARE DRIVER, LENGTH 42 SafetyFix Easy Out SAFETYFIX MEDICAL TECHNOLOGIES
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