510(k) K062341 ยท OTM Mesh, Surgical, For Stress Urinary Incontinence, Male
MALE REMEEX SYSTEM
| Applicant | Specialities Remeex International, S.L., Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 2, 2006 |
| Received | Aug 10, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062341
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.