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 "KWQ"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 03760178394871 VPCE-0019 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
2 03760178394864 PCEV-0022 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
3 03760178394857 A-TPC-0002-02 Instrument to use with ORIGIN implants Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
4 03760178394840 A-TPC-0002 Instrument to use with ORIGIN implants Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
5 03760178394833 A-TPC-0001 Instrument to use with ORIGIN implants Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
6 03760178394826 A-SQA-0025 Instrument to use with ORIGIN implants Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
7 03760178394802 A-CPL-0002 Instrument to use with ORIGIN implants Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
8 03760178391665 VREV-0017 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
9 03760178391658 VREV-0015 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
10 03760178391641 VREV-0013 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
11 03760178391634 VPCE-0017 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
12 03760178391627 VPCE-0015 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
13 03760178391610 VPCE-0013 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
14 03760178391528 PCEV-0034 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
15 03760178391511 PCEV-0031 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
16 03760178391504 PCEV-0028 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
17 03760178391498 PCEV-0026 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
18 03760178391481 PCEV-0024 Stabilize the bone fusion during the consolidation processus following the surgi Stabilize the bone fusion during the consolidation processus following the surgical correction of the spinal anomalies. Orthopaedic & Spine Development (OSD) ORTHOPAEDIC & SPINE DEVELOPMENT
19 03700780637850 43034020 43034020 AGGERIS-C VARIABLE SCREW Diameter 4.0x20MM SELF-DRILLING Aggeris™-C CLARIANCE
20 03700780637843 43034018 43034018 AGGERIS-C VARIABLE SCREW Diameter 4.0x18MM SELF-DRILLING Aggeris™-C CLARIANCE
21 03700780637836 43034016 43034016 AGGERIS-C VARIABLE SCREW Diameter 4.0x16MM SELF-DRILLING Aggeris™-C CLARIANCE
22 03700780637829 43034014 43034014 AGGERIS-C VARIABLE SCREW Diameter 4.0x14MM SELF-DRILLING Aggeris™-C CLARIANCE
23 03700780637812 43034012 43034012 AGGERIS-C VARIABLE SCREW Diameter 4.0x12MM SELF-DRILLING Aggeris™-C CLARIANCE
24 03700780637805 43044520 43044520 AGGERIS-C VARIABLE SCREW Diameter 4.5x20MM SELF-TAPPING Aggeris™-C CLARIANCE
25 03700780637799 43044518 43044518 AGGERIS-C VARIABLE SCREW Diameter 4.5x18MM SELF-TAPPING Aggeris™-C CLARIANCE
26 03700780637782 43044516 43044516 AGGERIS-C VARIABLE SCREW Diameter 4.5x16MM SELF-TAPPING Aggeris™-C CLARIANCE
27 03700780637775 43044514 43044514 AGGERIS-C VARIABLE SCREW Diameter 4.5x14MM SELF-TAPPING Aggeris™-C CLARIANCE
28 03700780637768 43044512 43044512 AGGERIS-C VARIABLE SCREW Diameter 4.5x12MM SELF-TAPPING Aggeris™-C CLARIANCE
29 03700780637751 43044510 43044510 AGGERIS-C VARIABLE SCREW Diameter 4.5x10MM SELF-TAPPING Aggeris™-C CLARIANCE
30 03700780637744 43044020 43044020 AGGERIS-C VARIABLE SCREW Diameter 4.0x20MM SELF-TAPPING Aggeris™-C CLARIANCE
31 03700780637737 43044018 43044018 AGGERIS-C VARIABLE SCREW Diameter 4.0x18MM SELF-TAPPING Aggeris™-C CLARIANCE
32 03700780637720 43044016 43044016 AGGERIS-C VARIABLE SCREW Diameter 4.0x16MM SELF-TAPPING Aggeris™-C CLARIANCE
33 03700780637713 43044014 43044014 AGGERIS-C VARIABLE SCREW Diameter 4.0x14MM SELF-TAPPING Aggeris™-C CLARIANCE
34 03700780637706 43044012 43044012 AGGERIS-C VARIABLE SCREW Diameter 4.0x12MM SELF-TAPPING Aggeris™-C CLARIANCE
35 03700780637690 43044010 43044010 AGGERIS-C VARIABLE SCREW Diameter 4.0x10MM SELF-TAPPING Aggeris™-C CLARIANCE
36 03700780637683 43054020 43054020 AGGERIS-C FIXED SCREW Diameter 4.0x20MM SELF-DRILLING Aggeris™-C CLARIANCE
37 03700780637676 43054018 43054018 AGGERIS-C FIXED SCREW Diameter 4.0x18MM SELF-DRILLING Aggeris™-C CLARIANCE
38 03700780637669 43054016 43054016 AGGERIS-C FIXED SCREW Diameter 4.0x16MM SELF-DRILLING Aggeris™-C CLARIANCE
39 03700780637652 43054014 43054014 AGGERIS-C FIXED SCREW Diameter 4.0x14MM SELF-DRILLING Aggeris™-C CLARIANCE
40 03700780637645 43054012 43054012 AGGERIS-C FIXED SCREW Diameter 4.0x12MM SELF-DRILLING Aggeris™-C CLARIANCE
41 03700780637638 43064520 43064520 AGGERIS-C FIXED SCREW Diameter 4.5x20MM SELF-TAPPING Aggeris™-C CLARIANCE
42 03700780637621 43064518 43064518 AGGERIS-C FIXED SCREW Diameter 4.5x18MM SELF-TAPPING Aggeris™-C CLARIANCE
43 03700780637614 43064516 43064516 AGGERIS-C FIXED SCREW Diameter 4.5x16MM SELF-TAPPING Aggeris™-C CLARIANCE
44 03700780637607 43064514 43064514 AGGERIS-C FIXED SCREW Diameter 4.5x14MM SELF-TAPPING Aggeris™-C CLARIANCE
45 03700780637591 43064512 43064512 AGGERIS-C FIXED SCREW Diameter 4.5x12MM SELF-TAPPING Aggeris™-C CLARIANCE
46 03700780637584 43064510 43064510 AGGERIS-C FIXED SCREW Diameter 4.5x10MM SELF-TAPPING Aggeris™-C CLARIANCE
47 03700780637577 43064020 43064020 AGGERIS-C FIXED SCREW Diameter 4.0x20MM SELF-TAPPING Aggeris™-C CLARIANCE
48 03700780637560 43064018 43064018 AGGERIS-C FIXED SCREW Diameter 4.0x18MM SELF-TAPPING Aggeris™-C CLARIANCE
49 03700780637553 43064016 43064016 AGGERIS-C FIXED SCREW Diameter 4.0x16MM SELF-TAPPING Aggeris™-C CLARIANCE
50 03700780637546 43064014 43064014 AGGERIS-C FIXED SCREW Diameter 4.0x14MM SELF-TAPPING Aggeris™-C CLARIANCE