510(k) K061704 ยท FTL Mesh, Surgical, Polymeric
OPTILENE MESH
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jul 19, 2006 |
| Received | Jun 16, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K061704
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.