No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00845694041133 | 395-4001-30 | 395-4001-30 | Tag, 0 Degree ExtremiFuse, 3.0 | HWC | Screw, fixation, bone | 2 | OsteoMed |
2 | 00845694041126 | 395-4001-24 | 395-4001-24 | Tag, 0 Degree ExtremiFuse, 2.4 | HWC | Screw, fixation, bone | 2 | OsteoMed |
3 | 00845694041119 | 395-4001-00 | 395-4001-00 | Tag, 0 Degree ExtremiFuse, Blank | HWC | Screw, fixation, bone | 2 | OsteoMed |
4 | 00845694041102 | 395-4000 | 395-4000 | ExtremiFuse Organizer Block | HWC | Screw, fixation, bone | 2 | OsteoMed |
5 | 00845694041096 | 395-2430 | 395-2430 | X-Ray Template, ExtremiFuse | HWC | Screw, fixation, bone | 2 | OsteoMed |
6 | 00845694041089 | 395-2200 | 395-2200 | ExtremiFuse Dual Cannulated Driver Handle | HWC | Screw, fixation, bone | 2 | OsteoMed |
7 | 00845694041072 | 395-2124 | 395-2124 | Broach, ExtremiFuse | HWC | Screw, fixation, bone | 2 | OsteoMed |
8 | 00845694041065 | 395-2027 | 395-2027 | Ø2.7mm Cannulated Drill, Quick Release | HWC | Screw, fixation, bone | 2 | OsteoMed |
9 | 00845694041058 | 395-2000 | 395-2000 | .035 x 3 K-Wire | HWC | Screw, fixation, bone | 2 | OsteoMed |
10 | 00845694041041 | 386-1705 | 386-1705 | Extraction System Tray | KWD | PROSTHESIS, TOE, HEMI-, PHALANGEAL | 2 | OsteoMed |
11 | 00845694041034 | 320-1029 | 320-1029 | Plate Bending Forceps, Large | HRS | Plate, fixation, bone | 2 | OsteoMed |
12 | 00845694041027 | 319-1030 | 319-1030 | 3.0mm x 10 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
13 | 00845694041010 | 319-1024 | 319-1024 | 2.4mm x 10 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
14 | 00845694041003 | 319-0030 | 319-0030 | 3.0mm x 0 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
15 | 00845694040990 | 319-0024 | 319-0024 | 2.4mm x 0 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
16 | 00845694040969 | 213-0127 | 213-0127 | 1.6mm, Left Zed Plate, 11mm | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
17 | 00845694040952 | 213-0126 | 213-0126 | 1.6mm, Right Zed Plate, 11mm | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
18 | 00845694040945 | 210-0255 | 210-0255 | 2.0mm Left L Plate, 23mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
19 | 00845694040938 | 210-0254 | 210-0254 | 2.0mm Right L Plate, 23mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
20 | 00845694040921 | 210-0253 | 210-0253 | 2.0mm Left L Plate, 18mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
21 | 00845694040914 | 210-0252 | 210-0252 | 2.0mm Right L Plate, 18mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
22 | 00845694040907 | 210-0251 | 210-0251 | 2.0mm Left L Plate, 15mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
23 | 00845694040891 | 210-0250 | 210-0250 | 2.0mm Right L Plate, 15mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
24 | 00845694040884 | 211-1606-REV-G | 211-1606-REV-G | 1.6mm x 6mm AUTO-DRIVE Screw | HWC | Screw, fixation, bone | 2 | OsteoMed |
25 | 00845694040877 | 213-0018-SP | 213-0018-SP | 1.6mm Rigid Curved Plate, 10 Hole, Sterile | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
26 | 00845694040860 | 212-0052-SP | 212-0052-SP | 19mm T Plate, Sterile | JEY | PLATE, BONE | 2 | OsteoMed |
27 | 00845694040853 | 212-0046-SP | 212-0046-SP | 13mm Right L Plate, Sterile | JEY | PLATE, BONE | 2 | OsteoMed |
28 | 00845694040846 | 212-0044-SP | 212-0044-SP | 13mm Left L Plate, Sterile | JEY | PLATE, BONE | 2 | OsteoMed |
29 | 00845694040839 | 212-0030-SP | 212-0030-SP | 7 Hole Y Plate, Sterile | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
30 | 00845694040822 | 213-0011-SP | 213-0011-SP | 10 Hole Curved Plate, Sterile | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
31 | 00845694040815 | 817-1017 | 817-1017 | PrimaLIF LLIF 17mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
32 | 00845694040808 | 817-1015 | 817-1015 | PrimaLIF LLIF 15mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
33 | 00845694040792 | 817-1013 | 817-1013 | PrimaLIF LLIF 13mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
34 | 00845694040785 | 817-1011 | 817-1011 | PrimaLIF LLIF 11mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
35 | 00845694040778 | 817-1009 | 817-1009 | PrimaLIF LLIF 9mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
36 | 00845694040761 | 817-1007 | 817-1007 | PrimaLIF LLIF 7mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
37 | 00845694040754 | 816-1017 | 816-1017 | PrimaLIF LLIF 17mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
38 | 00845694040747 | 816-1015 | 816-1015 | PrimaLIF LLIF 15mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
39 | 00845694040730 | 816-1013 | 816-1013 | PrimaLIF LLIF 13mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
40 | 00845694040723 | 816-1011 | 816-1011 | PrimaLIF LLIF 11mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
41 | 00845694040716 | 816-1009 | 816-1009 | PrimaLIF LLIF 9mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
42 | 00845694040709 | 816-1007 | 816-1007 | PrimaLIF LLIF 7mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
43 | 00845694040693 | 815-1017 | 815-1017 | PrimaLIF LLIF 17mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
44 | 00845694040686 | 815-1015 | 815-1015 | PrimaLIF LLIF 15mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
45 | 00845694040679 | 815-1013 | 815-1013 | PrimaLIF LLIF 13mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
46 | 00845694040662 | 815-1011 | 815-1011 | PrimaLIF LLIF 11mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
47 | 00845694040655 | 815-1009 | 815-1009 | PrimaLIF LLIF 9mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
48 | 00845694040648 | 815-1007 | 815-1007 | PrimaLIF LLIF 7mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
49 | 00845694040631 | 814-1017 | 814-1017 | PrimaLIF LLIF 17mm x 26mm Parallel Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
50 | 00845694040624 | 814-1015 | 814-1015 | PrimaLIF LLIF 15mm x 26mm Parallel Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00815362023686 | 50-0013 | 50-0013 | Facet Screw Tray (Empty) | Facet Screw System | PRECISION SPINE, INC. |
2 | 00815362023570 | 35-S5050-X | 35-S5050-X | 5.0 x 50mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
3 | 00815362023563 | 35-S5045-X | 35-S5045-X | 5.0 x 45mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
4 | 00815362023556 | 35-S5040-X | 35-S5040-X | 5.0 x 40mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
5 | 00815362023549 | 35-S5035-X | 35-S5035-X | 5.0 x 35mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
6 | 00815362023532 | 35-S5030-X | 35-S5030-X | 5.0 x 30mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
7 | 00815362023525 | 35-S5025-X | 35-S5025-X | 5.0 x 25mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
8 | 00815362023518 | 35-S4550-X | 35-S4550-X | 4.5 x 50mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
9 | 00815362023501 | 35-S4545-X | 35-S4545-X | 4.5 x 45mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
10 | 00815362023495 | 35-S4540-X | 35-S4540-X | 4.5 x 40mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
11 | 00815362023488 | 35-S4535-X | 35-S4535-X | 4.5 x 35mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
12 | 00815362023471 | 35-S4530-X | 35-S4530-X | 4.5 x 30mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
13 | 00815362023464 | 35-S4525-X | 35-S4525-X | 4.5 x 25mm Non-Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
14 | 00815362023457 | 35-S5050-K | 35-S5050-K | 5.0 x 50mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
15 | 00815362023440 | 35-S5045-K | 35-S5045-K | 5.0 x 45mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
16 | 00815362023433 | 35-S5040-K | 35-S5040-K | 5.0 x 40mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
17 | 00815362023426 | 35-S5035-K | 35-S5035-K | 5.0 x 35mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
18 | 00815362023419 | 35-S5030-K | 35-S5030-K | 5.0 x 30mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
19 | 00815362023402 | 35-S5025-K | 35-S5025-K | 5.0 x 25mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
20 | 00815362023396 | 35-S4550-K | 35-S4550-K | 4.5 x 50mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
21 | 00815362023389 | 35-S4545-K | 35-S4545-K | 4.5 x 45mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
22 | 00815362023372 | 35-S4540-K | 35-S4540-K | 4.5 x 40mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
23 | 00815362023365 | 35-S4535-K | 35-S4535-K | 4.5 x 35mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
24 | 00815362023358 | 35-S4530-K | 35-S4530-K | 4.5 x 30mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
25 | 00815362023341 | 35-S4525-K | 35-S4525-K | 4.5 x 25mm Cannulated Screw | Facet Screw System | PRECISION SPINE, INC. |
26 | 00815361020679 | TR1-2839 | 5.0 mm x 40 mm Vectre Facet Screw, Lag | Vectre | QUANDARY MEDICAL LLC | |
27 | 00815361020662 | TR1-2838 | 5.0 mm x 35 mm Vectre Facet Screw, Lag | Vectre | QUANDARY MEDICAL LLC | |
28 | 00815361020655 | TR1-2837 | 5.0 mm x 30 mm Vectre Facet Screw, Lag | Vectre | QUANDARY MEDICAL LLC | |
29 | 00815361020648 | TR1-2836 | 5.0 mm x 25 mm Vectre Facet Screw, Lag | Vectre | QUANDARY MEDICAL LLC | |
30 | 00815361020631 | TR1-2835 | 5.0 mm x 40 mm Vectre Facet Screw, Fully Threaded | Vectre | QUANDARY MEDICAL LLC | |
31 | 00815361020624 | TR1-2834 | 5.0 mm x 35 mm Vectre Facet Screw, Fully Threaded | Vectre | QUANDARY MEDICAL LLC | |
32 | 00815361020617 | TR1-2833 | 5.0 mm x 30 mm Vectre Facet Screw, Fully Threaded | Vectre | QUANDARY MEDICAL LLC | |
33 | 00815361020600 | TR1-2832 | 5.0 mm x 25 mm Vectre Facet Screw, Fully Threaded | Vectre | QUANDARY MEDICAL LLC | |
34 | 00815361020266 | 24-8003 | Vectre Screw Set, 40 mm (2 pk) with perm washer | Vectre | QUANDARY MEDICAL LLC | |
35 | 00815361020259 | 24-8002 | Vectre Screw Set, 35 mm (2 pk) with perm washer | Vectre | QUANDARY MEDICAL LLC | |
36 | 00815361020242 | 24-8001 | Vectre Screw Set, 30 mm (2 pk) with perm washer | Vectre | QUANDARY MEDICAL LLC | |
37 | 00815361020235 | 24-8000 | Vectre Screw Set, 25 mm (2 pk) with perm washer | Vectre | QUANDARY MEDICAL LLC | |
38 | 00813210022034 | 800-1213 | Threaded Implant Holder Shaft - Solid | primaLOK FF | WENZEL SPINE, INC. | |
39 | 00813210022027 | 800-1212 | Threaded Implant Holder Shaft - Cannulated | primaLOK FF | WENZEL SPINE, INC. | |
40 | 00813210022010 | 800-1211 | Implant Driver | primaLOK FF | WENZEL SPINE, INC. | |
41 | 00813210022003 | 800-1203 | Removal Driver | primaLOK FF | WENZEL SPINE, INC. | |
42 | 00813210021990 | 800-1145-00 | primaLOK FF 45mm Implant Assembly, Sterile primaLOK FF 45mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. | primaLOK FF | WENZEL SPINE, INC. | |
43 | 00813210021983 | 800-1140-00 | primaLOK FF 40mm Implant Assembly, Sterile primaLOK FF 40mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. | primaLOK FF | WENZEL SPINE, INC. | |
44 | 00813210021976 | 800-1135-00 | primaLOK FF 35mm Implant Assembly, Sterile primaLOK FF 35mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. | primaLOK FF | WENZEL SPINE, INC. | |
45 | 00813210021969 | 800-1130-00 | primaLOK FF 30mm Implant Assembly, Sterile primaLOK FF 30mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. | primaLOK FF | WENZEL SPINE, INC. | |
46 | 00813210021952 | 800-1125-00 | primaLOK FF 25mm Implant Assembly, Sterile primaLOK FF 25mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. | primaLOK FF | WENZEL SPINE, INC. | |
47 | 00811954013219 | LSW-45-4555 | 9024-02 | 4.5mm O.D. x 45-55mm Length | 4.5mm BONE-LOK PLS Implant | INTERVENTIONAL SPINE, INC |
48 | 00721902613371 | X0902440 | UCS DBLTHDSCR-TI-CANN-4.0X40 | UCSS® Screw Set | MEDTRONIC SOFAMOR DANEK, INC. | |
49 | 00721902319815 | 9098560 | 4.0 CORTICAL BONE SCREW 60MM | UCSS® Screw Set | MEDTRONIC SOFAMOR DANEK, INC. | |
50 | 00721902319792 | 9098558 | 4.0 CORTICAL BONE SCREW 58MM | UCSS® Screw Set | MEDTRONIC SOFAMOR DANEK, INC. |