510(k) K082640 ยท OTM Mesh, Surgical, For Stress Urinary Incontinence, Male
VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM
| Applicant | Coloplast Manufacturing Us, LLC, Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 17, 2008 |
| Received | Sep 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082640
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.