510(k) K021071 ยท FMF Syringe, Piston
PCCS GRAFT DELIVERY SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 1, 2002 |
| Received | Apr 2, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021071
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 4, 2007 | Biomet, Inc. Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Warsaw, Indiana; REF 800-0300. Terminated |
FMF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.