510(k) K062173 ยท FMF Syringe, Piston
MODIFICATION TO BONE GRAFT SYRINGE
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Aug 23, 2006 |
| Received | Jul 31, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062173
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.