510(k) K123206 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
MAXIM SURGICAL X-TREME INTERBODY FUSION SYSTEM
| Applicant | Maxim Surgical, Richardson TX, US |
| Decision | Substantially Equivalent, Feb 7, 2013 |
| Received | Oct 12, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123206
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.