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 "HWW"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 24026704276336 IPN014334 KM47924 COUNTERSINK 4 3/4" 3.2 MILLIMETER MALLEOLAR KMEDIC TELEFLEX INCORPORATED
2 10888551022989 SYN310.972 SYN310.972 COUNTERSINK NA STERILMED, INC.
3 10888551022972 SYN310.971 SYN310.971 COUNTERSINK NA STERILMED, INC.
4 10888551022965 SYN310.890 SYN310.890 COUNTERSINK FOR 3.5MM CORTEX AND 4.0MM CANCELLOUS BONE SCREWS NA STERILMED, INC.
5 10888551022958 SYN310.880 SYN310.880 COUNTERSINK FOR 1.5 & 2.0MM CORTEX SCREWS NA STERILMED, INC.
6 10888551022941 SYN310.870 SYN310.870 COUNTERSINK NA STERILMED, INC.
7 10888551022934 SYN310.86 SYN310.86 COUNTERSINK CANNULATED NA STERILMED, INC.
8 10888277355637 MSN20003RH MSN20003RH MSN20003 COUNTERSINK,3.0-3.5 HEADED,C Medline MEDLINE INDUSTRIES, INC.
9 10888277355620 MSN20001RH MSN20001RH MSN20001 COUNTERSINK,2.0-2.5 HEADED CA Medline MEDLINE INDUSTRIES, INC.
10 10888277355613 MSN20008RH MSN20008RH MSN20008 @COUNTERSINK, 6.5 HEADLESS, CAN Medline MEDLINE INDUSTRIES, INC.
11 10888277355606 MSN20007RH MSN20007RH MSN20007 @COUNTERSINK, 7.0 HEADED, CANTE Medline MEDLINE INDUSTRIES, INC.
12 10888277355590 MSN20005RH MSN20005RH MSN20005 COUNTERSINK,4.0-4.5 HEADED CA Medline MEDLINE INDUSTRIES, INC.
13 10888277355583 MSN20006RH MSN20006RH MSN20006 @COUNTERSINK, 4.5 HEADLESS, CAN Medline MEDLINE INDUSTRIES, INC.
14 10888277353541 MSN20004RH MSN20004RH MSN20004 @COUNTERSINK, 3.0 HEADLESS, CAN Medline MEDLINE INDUSTRIES, INC.
15 10886982300843 03.045.034S 03045034S COUNTERSINK / Ø 7.4MM QUICK COUPLING / STERILE NA SYNTHES (U.S.A.) LP
16 10886982300836 03.045.034 03045034 COUNTERSINK / Ø 7.4MM QUICK COUPLING NA SYNTHES GMBH
17 10886982187185 310.99 31099 COUNTERSINK FOR 4.5MM CORTEX SCREWS NA SYNTHES GMBH
18 10886982187178 310.972 310972 COUNTERSINK FOR 2.0MM/2.4MM SCREWS NA SYNTHES GMBH
19 10886982187161 310.971 310971 COUNTERSINK FOR 1.3MM/1.5MM SCREWS NA SYNTHES GMBH
20 10886982187154 310.96 31096 MALLEOLAR COUNTERSINK NA SYNTHES GMBH
21 10886982187062 310.89 31089 COUNTERSINK F/3.5MM CORTEX & 4.0MM CANCELLOUS BONE SCREWS NA SYNTHES GMBH
22 10886982187048 310.88 31088 COUNTERSINK F/1.5MM & 2.0MM CORTEX SCREWS NA SYNTHES GMBH
23 10886982187031 310.87 31087 COUNTERSINK FOR 2.7MM CORTEX SCREWS NA SYNTHES GMBH
24 10886982187024 310.86 31086 CANNULATED COUNTERSINK F/3.5MM & 4.0MM CANNULATED SCREWS NA SYNTHES GMBH
25 10886982187017 310.85 31085 CANNULATED COUNTERSINK FOR 4.5MM CANNULATED SCREWS NA SYNTHES GMBH
26 10886982187000 310.804 310804 CANNULATED COUNTERSINK FOR 3.0MM CANNULATED SCREWS NA SYNTHES GMBH
27 10886982186997 310.803 310803 CANNULATED COUNTERSINK FOR 2.4MM CANNULATED SCREWS NA SYNTHES GMBH
28 10886982186973 310.79 31079 CANNULATED COUNTERSINK FOR 7.0MM CANNULATED SCREWS NA SYNTHES GMBH
29 10886982186966 310.78 31078 CANNULATED COUNTERSINK FOR 6.5MM & 7.3MM CANN SCREWS NA SYNTHES GMBH
30 10886982075444 03.130.260 03130260 PLATE BENDING PLIERS F/1.3MM LCKNG/1.5-2.0MM VAL PLATES-RT NA SYNTHES GMBH
31 10886982075376 03.130.215 03130215 COUNTERSINK FOR 1.3MM/1.5MM AND 2.0MM SCREWS NA SYNTHES GMBH
32 10886982073952 03.119.026 03119026 CANN COUNTERSINK F/3.5MM & 4.0MM CANNULATED SCREWS/GREY NA SYNTHES GMBH
33 10886982073914 03.119.022 03119022 CANNULATED COUNTERSINK FOR 2.4MM CANN SCREWS/PURPLE NA SYNTHES GMBH
34 10886982073860 03.119.017 03119017 COUNTERSINK FOR 2.7MM CORTEX SCREWS/PURPLE/ORANGE NA SYNTHES GMBH
35 10886982073730 03.119.004 03119004 COUNTERSINK FOR 3.5 CORTEX AND 4.0 CANCELLOUS SCREWS/YELLOW NA SYNTHES GMBH
36 10885380083228 CH04-0010 CH04-0010 Countersink 3.5mm Cortex/4.0mm Cancellous Bone Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
37 10885380083211 CH04-0006 CH04-0006 Countersink 2.7mm Cortex Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
38 10885380083204 CH04-0009 CH04-0009 Countersink 2.0mm/2.4mm Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
39 10885380083198 CH04-0007 CH04-0007 Countersink 1.5mm/2.0mm Cortex Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
40 10885380083181 CH04-0008 CH04-0008 Countersink 1.3mm/1.5mm Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
41 10885380083020 CH04-0005 CH04-0005 Cannulated Countersink 6.5mm/7.3mm Cannulated Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
42 10885380083013 CH04-0004 CH04-0004 Cannulated Countersink 4.5mm Cannulated Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
43 10885380083006 CH04-0003 CH04-0003 Cannulated Countersink 3.0mm Cannulated Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
44 10885380082993 CH04-0002 CH04-0002 Cannulated Countersink 2.4mm Cannulated Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
45 10885380082986 CH04-0001 CH04-0001 Cannulated Countersink 3.5mm/4.0mm Cannulated Screws CARDINAL HEALTH CARDINAL HEALTH 200, LLC
46 M695HTR040092470 HTR-04-009247 HTR-04-009247 6.5 Screw Countersink Orion Headed Screw System Instruments TYBER MEDICAL LLC
47 M695HTR040091430 HTR-04-009143 HTR-04-009143 4.5 Screw Countersink Orion Headed Screw System Instruments TYBER MEDICAL LLC
48 M695HTR040091400 HTR-04-009140 HTR-04-009140 2.5 / 3.0 Screw Countersink Orion Headed Screw System Instruments TYBER MEDICAL LLC
49 M695HTR040091380 HTR-04-009138 HTR-04-009138 2.0 Headed Screw Countersink Orion Headed Screw System Instruments TYBER MEDICAL LLC
50 M6950090000500 009-000050 009-000050 9.0 Screw Countersink Headed Screw System Instruments TYBER MEDICAL LLC