510(k) K093932 ยท FTL Mesh, Surgical, Polymeric
ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH
| Applicant | Ethicon GmbH, Sommerville NJ, US |
| Decision | Substantially Equivalent, Apr 9, 2010 |
| Received | Dec 22, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093932
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.