510(k) K770405 ยท IRN Device, Warning, Overload, External Limb, Powered
OVERLOAD WARNING DEVICE
| Applicant | Synthes (Usa), Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 10, 1977 |
| Received | Mar 3, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770405
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.