510(k) K130853 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
IDYS(TM) C
| Applicant | Clariance, Philedelphia PA, US |
| Decision | Substantially Equivalent, Nov 13, 2013 |
| Received | Mar 28, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130853
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.