The following data is part of a premarket notification filed by Ethicon, Inc. with the FDA for Gynecare Tvt Exact Continence System.
Device ID | K100485 |
510k Number | K100485 |
Device Name: | GYNECARE TVT EXACT CONTINENCE SYSTEM |
Classification | Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator |
Applicant | ETHICON, INC. ROUTE 22 WEST Somerville, NJ 08876 -0151 |
Contact | Susan Lin |
Correspondent | Susan Lin ETHICON, INC. ROUTE 22 WEST Somerville, NJ 08876 -0151 |
Product Code | OTN |
CFR Regulation Number | 878.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-02-19 |
Decision Date | 2010-03-16 |
Summary: | summary |