No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00887517399779 | 6942044 | CoRoent® XLR, 20x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
2 | 00887517399700 | 6941844 | CoRoent® XLR, 18x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
3 | 00887517399335 | 6941644 | CoRoent® XLR, 16x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
4 | 00887517398765 | 6941444 | CoRoent® XLR, 14x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
5 | 00887517398499 | 6941244 | CoRoent® XLR, 12x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
6 | 00887517398420 | 6941044 | CoRoent® XLR, 10x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
7 | 00887517398055 | 6932088 | CoRoent® XLR, 20x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
8 | 00887517397683 | 6931888 | CoRoent® XLR, 18x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
9 | 00887517397256 | 6931688 | CoRoent® XLR, 16x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
10 | 00887517396822 | 6931488 | CoRoent® XLR, 14x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
11 | 00887517396457 | 6931288 | CoRoent® XLR, 12x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
12 | 00887517395641 | 6922088 | CoRoent® XLR, 20x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
13 | 00887517395634 | 6922044 | CoRoent® XLR, 20x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
14 | 00887517395269 | 6921888 | CoRoent® XLR, 18x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
15 | 00887517395252 | 6921844 | CoRoent® XLR, 18x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
16 | 00887517394880 | 6921688 | CoRoent® XLR, 16x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
17 | 00887517394873 | 6921660 | CoRoent® XL Wide, 16x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
18 | 00887517394866 | 6921655 | CoRoent® XL Wide, 16x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
19 | 00887517394859 | 6921650 | CoRoent® XL Wide, 16x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
20 | 00887517394842 | 6921645 | CoRoent® XL Wide, 16x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
21 | 00887517394835 | 6921644 | CoRoent® XLR, 16x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
22 | 00887517394569 | 6921488 | CoRoent® XLR, 14x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
23 | 00887517394552 | 6921460 | CoRoent® XL Wide, 14x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
24 | 00887517394545 | 6921455 | CoRoent® XL Wide, 14x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
25 | 00887517394538 | 6921450 | CoRoent® XL Wide, 14x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
26 | 00887517394521 | 6921445 | CoRoent® XL Wide, 14x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
27 | 00887517394514 | 6921444 | CoRoent® XLR, 14x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
28 | 00887517394149 | 6921288 | CoRoent® XLR, 12x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
29 | 00887517394132 | 6921260 | CoRoent® XL Wide, 12x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
30 | 00887517394125 | 6921255 | CoRoent® XL Wide, 12x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
31 | 00887517394118 | 6921250 | CoRoent® XL Wide, 12x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
32 | 00887517394101 | 6921245 | CoRoent® XL Wide, 12x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
33 | 00887517393791 | 6921244 | CoRoent® XLR, 12x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
34 | 00887517393722 | 6921088 | CoRoent® XLR, 10x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
35 | 00887517393715 | 6921060 | CoRoent® XL Wide, 10x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
36 | 00887517393708 | 6921055 | CoRoent® XL Wide, 10x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
37 | 00887517393395 | 6921050 | CoRoent® XL Wide, 10x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
38 | 00887517393388 | 6921045 | CoRoent® XL Wide, 10x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
39 | 00887517393371 | 6921044 | CoRoent® XLR, 10x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
40 | 00887517393333 | 6920860 | CoRoent® XL Wide, 8x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
41 | 00887517393326 | 6920855 | CoRoent® XL Wide, 8x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
42 | 00887517393319 | 6920850 | CoRoent® XL Wide, 8x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
43 | 00887517393302 | 6920845 | CoRoent® XL Wide, 8x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
44 | 00887517392961 | 6916860 | CoRoent® XL, 16x18x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
45 | 00887517392954 | 6916855 | CoRoent® XL, 16x18x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
46 | 00887517392947 | 6916850 | CoRoent® XL, 16x18x50mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
47 | 00887517392930 | 6916845 | CoRoent® XL, 16x18x45mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
48 | 00887517392923 | 6916840 | CoRoent® XL, 16x18x40mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
49 | 00887517392916 | 6916260 | CoRoent® XL Wide, 16x22x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
50 | 00887517392909 | 6916255 | CoRoent® XL Wide, 16x22x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent |
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. |