RESURFACE PROSHESIS
| Applicant | Aesculap Instruments Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 27, 1978 |
| Received | Aug 4, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781343
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.