510(k) K082926 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ZUMA, MODEL 55-XXXX/56-XXXX
| Applicant | Seaspine, Inc., Vista CA, US |
| Decision | Substantially Equivalent, Dec 22, 2008 |
| Received | Oct 1, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082926
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.