510(k) K122518 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
SYNSTER (CERVICAL,ALIF, PLIF, PTLIF AND TLIF) CAGE HERA CERVICAL CAGE RHEA PLIF CAGE TALON TIFA CAGE
| Applicant | Bm Korea Co., Ltd., Fullerton CA, US |
| Decision | Substantially Equivalent, Feb 15, 2013 |
| Received | Aug 17, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122518
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.