510(k) K953806 ยท JEY Plate, Bone
SYNTHES (USA) MIDFACIAL SYSTEM
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Mar 8, 1996 |
| Received | Aug 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953806
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.