No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | M711CRT006ST0 | CRT006ST | CP Ti | GWO | Plate, Cranioplasty, Preformed, Alterable | 2 | Neuro & Craniofacial Fixation System | |
2 | M711E20024 | E2002 | E2002 | KWQ,KWP,MNH,MNI,NKB | Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Inte Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease | Excella II® | ||
3 | M711BTA1190 | BTA-119 | Al, SST, Nylon, Silicone | LXH | Orthopedic Manual Surgical Instrument | 1 | PSO | |
4 | M711X212163200 | X21216320 | X21216320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
5 | M711X212163000 | X21216300 | X21216300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
6 | M711X212162800 | X21216280 | X21216280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
7 | M711X212153200 | X21215320 | X21215320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
8 | M711X212153000 | X21215300 | X21215300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
9 | M711X212152800 | X21215280 | X21215280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
10 | M711X212143200 | X21214320 | X21214320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
11 | M711X212143000 | X21214300 | X21214300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
12 | M711X212142800 | X21214280 | X21214280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
13 | M711X212133200 | X21213320 | X21213320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
14 | M711X212133000 | X21213300 | X21213300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
15 | M711X212132800 | X21213280 | X21213280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
16 | M711X212123200 | X21212320 | X21212320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
17 | M711X212123000 | X21212300 | X21212300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
18 | M711X212122800 | X21212280 | X21212280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
19 | M711X212113200 | X21211320 | X21211320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
20 | M711X212113000 | X21211300 | X21211300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
21 | M711X212112800 | X21211280 | X21211280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
22 | M711X212103200 | X21210320 | X21210320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
23 | M711X212103000 | X21210300 | X21210300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
24 | M711X212102800 | X21210280 | X21210280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
25 | M711X212093200 | X21209320 | X21209320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
26 | M711X212093000 | X21209300 | X21209300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
27 | M711X212092800 | X21209280 | X21209280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
28 | M711X212082800 | X21208280 | X21208280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
29 | M711X210162550 | X21016255 | X21016255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
30 | M711X210162500 | X21016250 | X21016250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
31 | M711X210162250 | X21016225 | X21016225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
32 | M711X210162200 | X21016220 | X21016220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
33 | M711X210153200 | X21015320 | X21015320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
34 | M711X210152800 | X21015280 | X21015280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
35 | M711X210152550 | X21015255 | X21015255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
36 | M711X210152500 | X21015250 | X21015250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
37 | M711X210152250 | X21015225 | X21015225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
38 | M711X210152200 | X21015220 | X21015220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
39 | M711X210143200 | X21014320 | X21014320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
40 | M711X210142800 | X21014280 | X21014280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
41 | M711X210142550 | X21014255 | X21014255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
42 | M711X210142500 | X21014250 | X21014250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
43 | M711X210142250 | X21014225 | X21014225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
44 | M711X210142200 | X21014220 | X21014220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
45 | M711X210133200 | X21013320 | X21013320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
46 | M711X210132800 | X21013280 | X21013280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
47 | M711X210132550 | X21013255 | X21013255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
48 | M711X210132500 | X21013250 | X21013250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
49 | M711X210132250 | X21013225 | X21013225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
50 | M711X210132200 | X21013220 | X21013220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
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. |