510(k) K082730 ยท OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed
AMS ELEVATE APICAL AND POSTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE, AMS ELEVATE APICAL AND POSTERIOR PROLAPSE
| Applicant | American Medical Systems, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Nov 26, 2008 |
| Received | Sep 18, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082730
No recall in the FDA data names this 510(k).
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