510(k) K083467 ยท FTL Mesh, Surgical, Polymeric
REBOUND HRDV
| Applicant | Minnesota Medical Development, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Apr 23, 2009 |
| Received | Nov 24, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K083467
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.