510(k) K990965 ยท KWP Appliance, Fixation, Spinal Interlaminal
SYNTHES CERVIFIX SYSTEM
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Jul 1, 1999 |
| Received | Mar 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990965
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.