510(k) K023675 ยท KWP Appliance, Fixation, Spinal Interlaminal
SYNTHES CERVIFIX/ AXON
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Nov 26, 2002 |
| Received | Nov 1, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023675
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.