510(k) K072951 ยท OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed
PARIETENE DUO AND QUADRA POLYPROPYLENE MESHES
| Applicant | Sofradim Production, Norwalk CT, US |
| Decision | Substantially Equivalent, Dec 19, 2007 |
| Received | Oct 18, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072951
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.