510(k) K071512 ยท OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed
GYNECARE PROLIFT +M* PELVIC FLOOR REPAIR SYSTEMS
| Applicant | ETHICON, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, May 15, 2008 |
| Received | Jun 4, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071512
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.