meddevicedb.com FDA Device Reference

MONOCRYL PLUS ANTIBACTERIAL SUTURE

K050845 Class II Traditional
Decision Date
2005-06-29
Sponsor / Applicant
ETHICON, Inc.

Technical Specification

510(k) Submission ID K050845
Product Code GAM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4493
Decision Date 2005-06-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MONOCRYL PLUS ANTIBACTERIAL SUTURE received FDA 510(k) clearance under submission number K050845, sponsored by ETHICON, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2005-06-29.

Classification & Regulation

This clearance is catalogued under FDA product code GAM and 21 CFR 878.4493, within the General, Plastic Surgery review panel as a Class II device.