510(k) K063739 ยท FTL Mesh, Surgical, Polymeric
SEPRAMESH, MODEL 5959-1214
| Applicant | Genzyme Corporation, Cambridge MA, US |
| Decision | Substantially Equivalent, Jan 17, 2007 |
| Received | Dec 18, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063739
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.