The following data is part of a premarket notification filed by American Medical Systems, Inc. with the FDA for Monarc + Subfascial Hammock, Model 72404193; Monarc C Subfascial Hammock, Model 72404195..
Device ID | K051530 |
510k Number | K051530 |
Device Name: | MONARC + SUBFASCIAL HAMMOCK, MODEL 72404193; MONARC C SUBFASCIAL HAMMOCK, MODEL 72404195. |
Classification | Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator |
Applicant | AMERICAN MEDICAL SYSTEMS, INC. 10700 BREN RD., WEST Minnetonka, MN 55343 |
Contact | Denise Thompson |
Correspondent | Denise Thompson AMERICAN MEDICAL SYSTEMS, INC. 10700 BREN RD., WEST Minnetonka, MN 55343 |
Product Code | OTN |
CFR Regulation Number | 878.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-06-09 |
Decision Date | 2005-07-08 |
Summary: | summary |