510(k) K062413 ยท HAD Rongeur, Powered
AESCULAP PNEUMATIC KERRISON
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Nov 21, 2006 |
| Received | Aug 17, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062413
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.