510(k) K892411 ยท JDQ Cerclage, Fixation
MENNEN BONE FIXATION DEVICE
| Applicant | Dentsply Intl., York PA, US |
| Decision | Substantially Equivalent, Jan 5, 1990 |
| Received | Apr 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892411
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.