meddevicedb.com FDA Device Reference

USSC POLYSORB SUTURE

K951520 Class II Traditional
Decision Date
1995-08-21
Sponsor / Applicant
United States Surgical, A Division of Tyco Healthc

Technical Specification

510(k) Submission ID K951520
Product Code GAM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4493
Decision Date 1995-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

USSC POLYSORB SUTURE received FDA 510(k) clearance under submission number K951520, 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 1995-08-21.

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.