meddevicedb.com FDA Device Reference

AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE

K934720 Class II Traditional
Decision Date
1994-03-25
Sponsor / Applicant
United States Surgical, A Division of Tyco Healthc

Technical Specification

510(k) Submission ID K934720
Product Code HRX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1100
Decision Date 1994-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE received FDA 510(k) clearance under submission number K934720, sponsored by United States Surgical, A Division of Tyco Healthc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1994-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code HRX and 21 CFR 888.1100, within the Orthopedic review panel as a Class II device.