510(k) K974540 ยท FTL Mesh, Surgical, Polymeric
SIS HERNIA REPAIR DEVICE
| Applicant | Sentron Medical, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, May 20, 1998 |
| Received | Dec 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974540
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.