510(k) K991089 ยท KWP Appliance, Fixation, Spinal Interlaminal
SYNTHES CERVIFIX SYSTEM
| Applicant | Synthes Spine, Paoli PA, US |
| Decision | Substantially Equivalent, Aug 27, 1999 |
| Received | Mar 31, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991089
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.