510(k) K121253 ยท HBF Drills, Burrs, Trephines & Accessories (Compound, Powered)
MERIDIAN CRANIAL PERFORATOR
| Applicant | Adeor Medical Technologies GmbH, Pullach, DE |
| Decision | Substantially Equivalent, Jul 17, 2012 |
| Received | Apr 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121253
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.