510(k) K072330 ยท FMF Syringe, Piston
CONTROLLED DELIVERY FOR OSTEOPLASTY (CDO SYSTEM) AND GRAFT PREPARATION SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Dec 6, 2007 |
| Received | Aug 20, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072330
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.