510(k) K113252 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
PEEK PREVAIL CERVICAL INTERBODY DEVICE
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Jan 17, 2012 |
| Received | Nov 3, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113252
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.