Other products from "SAFE ORTHOPAEDICS"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 03760219919650 KITMC725 NKB Thoracolumbosacral Pedicle Screw System 2 STERISPINE PS
2 03760219912026 KITMCL535 NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease 2 STERISPINE PS
3 03760219912002 KITMCL530 NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease 2 STERISPINE PS
4 03760219911517 KITM545 NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease 2 STERISPINE PS
5 03760219910787 KITM585 NKB Thoracolumbosacral Pedicle Screw System 2 STERISPINE PS
6 03760219910480 KITM565 NKB Thoracolumbosacral Pedicle Screw System 2 STERISPINE PS
7 03760219910046 KITM540 NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease 2 STERISPINE PS
8 03760219910039 KITM535 NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease 2 STERISPINE PS
9 03760219919254 KITLCS24-07 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
10 03760219919247 KITLCS24-08 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
11 03760219919230 KITLCS24-09 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
12 03760219919223 KITLCS24-10 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
13 03760219919216 KITLCS24-11 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
14 03760219919209 KITLCS24-12 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
15 03760219919193 KITLCS24-13 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
16 03760219919186 KITLCS24-14 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
17 03760219919179 KITLCS26-07 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
18 03760219919162 KITLCS26-08 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
19 03760219919155 KITLCS26-09 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
20 03760219919148 KITLCS26-10 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
21 03760219919131 KITLCS26-11 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
22 03760219919124 KITLCS26-12 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
23 03760219919117 KITLCS26-13 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
24 03760219919100 KITLCS26-14 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
25 03760219919094 KITLCS30-07 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
26 03760219919087 KITLCS30-08 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
27 03760219919070 KITLCS30-09 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
28 03760219919063 KITLCS30-10 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
29 03760219919056 KITLCS30-11 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
30 03760219919049 KITLCS30-12 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
31 03760219919032 KITLCS30-13 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
32 03760219919025 KITLCS30-14 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
33 03760219913047 KITANCLC 2 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
34 03760219912613 KITLCS32-14 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
35 03760219912606 KITLCS32-13 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
36 03760219912590 KITLCS32-12 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
37 03760219912583 KITLCS32-11 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
38 03760219912576 KITLCS32-10 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
39 03760219912569 KITLCS32-09 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
40 03760219912552 KITLCS32-08 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
41 03760219912545 KITLCS32-07 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
42 03760219912538 KITLCC32-14 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
43 03760219912521 KITLCC32-13 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
44 03760219912514 KITLCC32-12 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
45 03760219912507 KITLCC32-11 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
46 03760219912491 KITLCC32-10 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
47 03760219912484 KITLCC32-09 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
48 03760219912477 KITLCC32-08 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
49 03760219912460 KITLCC32-07 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
50 03760219912453 KITLCC30-14 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 STERISPINE LC
Other products with the same Product Code "MAX"
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.