510(k) K173501 ยท PWK Instrumentation, Surgical Mesh, Urogynecologic, Transabdominal Repair Of Pelvic Organ Prolapse
Meridian Vaginal Positioning System (VPS)
| Applicant | Coloplast, Plymouth MN, US |
| Decision | Substantially Equivalent, Feb 9, 2018 |
| Received | Nov 13, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173501
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.