meddevicedb.com FDA Device Reference

ABSORBABLE SURGICAL GUT SUTURE*

K885018 Class II Traditional
Decision Date
1989-08-22
Sponsor / Applicant
United States Surgical, A Division of Tyco Healthc

Technical Specification

510(k) Submission ID K885018
Product Code GAL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4830
Decision Date 1989-08-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABSORBABLE SURGICAL GUT SUTURE* received FDA 510(k) clearance under submission number K885018, sponsored by United States Surgical, A Division of Tyco Healthc. 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 1989-08-22.

Classification & Regulation

This clearance is catalogued under FDA product code GAL and 21 CFR 878.4830, within the General, Plastic Surgery review panel as a Class II device.