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 | 10889910058434 | 33-2007 | 33-2007 | Pacifica-S Implant, 9mm x 20mm x 7mm | SeaSpine Spacer System - Pacifica™ | SEASPINE ORTHOPEDICS CORPORATION |
2 | 10888857556041 | PRO-1255-16 | PRO-1255-16 | Cervical Disc Trial Size 13x16x12 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
3 | 10888857556034 | PRO-1255-15 | PRO-1255-15 | Cervical Disc Trial Size 13x16x11 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
4 | 10888857556027 | PRO-1255-14 | PRO-1255-14 | Cervical Disc Trial Size 13x16x10 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
5 | 10888857556010 | PRO-1255-13 | PRO-1255-13 | Cervical Disc Trial Size 13x16x9 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
6 | 10888857556003 | PRO-1255-12 | PRO-1255-12 | Cervical Disc Trial Size 13x16x8 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
7 | 10888857555990 | PRO-1255-11 | PRO-1255-11 | Cervical Disc Trial Size 13x16x7 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
8 | 10888857555983 | PRO-1255-10 | PRO-1255-10 | Cervical Disc Trial Size 13x16x6 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
9 | 10888857555976 | PRO-1255-09 | PRO-1255-09 | Cervical Disc Trial Size 13x16x5 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
10 | 10888857555969 | PRO-1255-08 | PRO-1255-08 | Cervical Disc Trial Size 12x14x12 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
11 | 10888857555952 | PRO-1255-07 | PRO-1255-07 | Cervical Disc Trial Size 12x14x11 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
12 | 10888857555945 | PRO-1255-06 | PRO-1255-06 | Cervical Disc Trial Size 12x14x10 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
13 | 10888857555938 | PRO-1255-05 | PRO-1255-05 | Cervical Disc Trial Size 12x14x9 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
14 | 10888857555921 | PRO-1255-04 | PRO-1255-04 | Cervical Disc Trial Size 12x14x8 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
15 | 10888857555914 | PRO-1255-03 | PRO-1255-03 | Cervical Disc Trial Size 12x14x7 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
16 | 10888857555907 | PRO-1255-02 | PRO-1255-02 | Cervical Disc Trial Size 12x14x6 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
17 | 10888857555891 | PRO-1255-01 | PRO-1255-01 | Cervical Disc Trial Size 12x14x5 mm, 7° | ALEUTIAN Interbody Systems | K2M, INC. |
18 | 10888857554740 | PRO-1238-20 | PRO-1238-20 | Trial Size 16x20x15 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
19 | 10888857554733 | PRO-1238-19 | PRO-1238-19 | Trial Size 16x20x14 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
20 | 10888857554726 | PRO-1238-18 | PRO-1238-18 | Trial Size 16x20x13 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
21 | 10888857554719 | PRO-1238-17 | PRO-1238-17 | Trial Size 16x20x12 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
22 | 10888857554702 | PRO-1238-16 | PRO-1238-16 | Trial Size 16x20x11 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
23 | 10888857554696 | PRO-1238-15 | PRO-1238-15 | Trial Size 16x20x10 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
24 | 10888857554689 | PRO-1238-14 | PRO-1238-14 | Trial Size 16x20x9 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
25 | 10888857554672 | PRO-1238-13 | PRO-1238-13 | Trial Size 16x20x8 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
26 | 10888857554665 | PRO-1238-12 | PRO-1238-12 | Trial Size 16x20x7 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
27 | 10888857554658 | PRO-1238-11 | PRO-1238-11 | Trial Size 16x20x6 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
28 | 10888857554641 | PRO-1238-10 | PRO-1238-10 | Trial Size 14x18x15 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
29 | 10888857554634 | PRO-1238-09 | PRO-1238-09 | Trial Size 14x18x14 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
30 | 10888857554627 | PRO-1238-08 | PRO-1238-08 | Trial Size 14x18x13 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
31 | 10888857554610 | PRO-1238-07 | PRO-1238-07 | Trial Size 14x18x12 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
32 | 10888857554603 | PRO-1238-06 | PRO-1238-06 | Trial Size 14x18x11 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
33 | 10888857554597 | PRO-1238-05 | PRO-1238-05 | Trial Size 14x18x10 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
34 | 10888857554580 | PRO-1238-04 | PRO-1238-04 | Trial Size 14x18x9 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
35 | 10888857554573 | PRO-1238-03 | PRO-1238-03 | Trial Size 14x18x8 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
36 | 10888857554566 | PRO-1238-02 | PRO-1238-02 | Trial Size 14x18x7 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
37 | 10888857554559 | PRO-1238-01 | PRO-1238-01 | Trial Size 14x18x6 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
38 | 10888857549159 | PRO-1167-02 | PRO-1167-02 | Inserter Inner Shaft | ALEUTIAN® Interbody Systems | K2M, INC. |
39 | 10888857549142 | PRO-1167-01 | PRO-1167-01 | Adjustable Inserter | ALEUTIAN® Interbody Systems | K2M, INC. |
40 | 10888857548794 | PRO-1165-02 | PRO-1165-02 | Inner Shaft | CASCADIA™ Interbody System | K2M, INC. |
41 | 10888857548763 | PRO-1161-01 | PRO-1161-01 | Trial Inserter | ALEUTIAN® Interbody Systems | K2M, INC. |
42 | 10888857528260 | PRO-1109 | PRO-1109 | Trial Inserter Size 25° | ALEUTIAN® Interbody Systems | K2M, INC. |
43 | 10888857525061 | PRO-1093-11 | PRO-1093-11 | Trial With Stop Size 12x14x15 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
44 | 10888857525054 | PRO-1093-10 | PRO-1093-10 | Trial With Stop Size 12x14x14 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
45 | 10888857525047 | PRO-1093-09 | PRO-1093-09 | Trial With Stop Size 12x14x13 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
46 | 10888857525030 | PRO-1093-08 | PRO-1093-08 | Trial With Stop Size12x14x12 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
47 | 10888857525023 | PRO-1093-07 | PRO-1093-07 | Trial With Stop Size 12x14x11 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
48 | 10888857525016 | PRO-1093-06 | PRO-1093-06 | Trial With Stop Szie 12x14x10 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
49 | 10888857525009 | PRO-1093-05 | PRO-1093-05 | Trial With Stop Size12x14x9 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
50 | 10888857524996 | PRO-1093-04 | PRO-1093-04 | Trial With Stop Size 12x14x8 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |