510(k) K062697 ยท FTL Mesh, Surgical, Polymeric
SIS HERNIA REPAIR DEVICE, SURGISIS GOLD HERNIA REPAIR GRAFT
| Applicant | Cook Biotech, Inc., West Lafayette IN, US |
| Decision | Substantially Equivalent, Oct 13, 2006 |
| Received | Sep 11, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062697
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.