510(k) K063671 ยท FTL Mesh, Surgical, Polymeric
REBOUND HRD
| Applicant | Minnesota Medical Development, Inc., Stillwater MN, US |
| Decision | Substantially Equivalent, Aug 16, 2007 |
| Received | Dec 11, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063671
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.