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AUTO SUTURE PREMIUM PLUS CEEA DISPOSABLE STAPLER

K020804 Class II Traditional
Decision Date
2002-11-19
Sponsor / Applicant
United States Surgical, A Division of Tyco Healthc

Technical Specification

510(k) Submission ID K020804
Product Code GDW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4750
Decision Date 2002-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO SUTURE PREMIUM PLUS CEEA DISPOSABLE STAPLER received FDA 510(k) clearance under submission number K020804, 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 2002-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code GDW and 21 CFR 878.4750, within the General, Plastic Surgery review panel as a Class II device.