Cleared Traditional

K132580 - COATED VICRYL PLUS ANTIMICROBIAL (POLYGLACTIN 910) SYNTHETIC ABSORBABLE SUTURE (FDA 510(k) Clearance)

Feb 2014
Decision
196d
Days
Class 2
Risk

K132580 is an FDA 510(k) clearance for the COATED VICRYL PLUS ANTIMICROBIAL (POLYGLACTIN 910) SYNTHETIC ABSORBABLE SUTURE. This device is classified as a Suture, Absorbable, Synthetic, Polyglycolic Acid (Class II - Special Controls, product code GAM).

Submitted by Ethicon, Inc. (Somerville, US). The FDA issued a Cleared decision on February 28, 2014, 196 days after receiving the submission on August 16, 2013.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4493.

Submission Details

510(k) Number K132580 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 16, 2013
Decision Date February 28, 2014
Days to Decision 196 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code GAM — Suture, Absorbable, Synthetic, Polyglycolic Acid
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4493