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 "NKB"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
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6 20643169490660 5535ROD2PER ROD 5535ROD2PER PRE-BENT 5.5X35 TI STER CD HORIZON ESSENTIALS™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
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9 20643169210183 7078396 SET SCREW 7078396 5.5/6.0 TI BO 4 PK CD Horizon® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
10 20613994170174 99465135 CAP 99465135 THREADED NUT CAP SI CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
11 18257200131952 36-5630SP 6.5MM X 30MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
12 18257200131945 36-5455SP 4.5MM X 55MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
13 18257200131938 36-5450SP 4.5MM X 50MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
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16 18257200131907 36-5435SP 4.5MM X 35MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
17 18257200131891 36-5430SP 4.5MM X 30MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
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29 18257200131754 36-6333 TALL ADAPTER CADDY FENESTRATED SCREWS ORTHOFIX INC.
30 18257200131747 36-6322 SHORT ADAPTER CADDY FENESTRATED SCREWS ORTHOFIX INC.
31 18257200131730 36-6321 CANNULA CADDY FENESTRATED SCREWS ORTHOFIX INC.
32 18257200131723 36-6320 BOTTOM LEVEL, JANUS FENESTRATED IMPLANT & INSTRUMENT CASE FENESTRATED SCREWS ORTHOFIX INC.
33 18257200131716 36-6316 9.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
34 18257200131709 36-6315 8.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
35 18257200131693 36-6314 7.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
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37 18257200131679 36-6312 5.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
38 18257200131662 36-6311 4.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
39 18257200131655 36-6310 TOP LEVEL, JANUS FENESTRATED IMPLANT & INSTRUMENT CASE FENESTRATED SCREWS ORTHOFIX INC.
40 18257200131648 36-6300B BASE, JANUS FENESTRATED IMPLANT & INSTRUMENT CASE FENESTRATED SCREWS ORTHOFIX INC.
41 18257200131631 36-6300 JANUS FENESTRATED IMPLANT & INSTRUMENT CASE FENESTRATED SCREWS ORTHOFIX INC.
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46 18257200129782 36-5935SP 9.5MM X 35MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
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48 18257200129713 36-5855SP 8.5MM X 55MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
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