510(k) K092521 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
ZUMA-C
| Applicant | Seaspine, Inc., Vista CA, US |
| Decision | Substantially Equivalent, Apr 13, 2010 |
| Received | Aug 18, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092521
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.