510(k) K033636 ยท OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed
AMS LARGE PORE POLYPROPYLENE MESH
| Applicant | American Medical Systems, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Dec 31, 2003 |
| Received | Nov 19, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033636
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.