510(k) K091722 ยท FMF Syringe, Piston
COAXIAL APPLICATOR SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Mar 12, 2010 |
| Received | Jun 11, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091722
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.