510(k) K092207 ยท OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed
RESTORELLE POLYPROPYLENE MESH
| Applicant | Mpathy Medical Devices, Inc., Glasgow, GB |
| Decision | Substantially Equivalent, Aug 4, 2009 |
| Received | Jul 22, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092207
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.