510(k) K242473 ยท PAH Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-Sling
Altis Single Incision Sling System (519650); Aris Transobturator Sling System (519551); Supris Retropubic Sling System (519562)
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 18, 2024 |
| Received | Aug 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242473
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.