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MEDTRONIC INSTENT ESOPHACOIL ESOPHAGEAL STENT SYSTEM AND ESOPHACOIL EXTENSION SYSTEM

K973584 Class II Traditional
Decision Date
1998-01-09
Sponsor / Applicant
Medtech Instruments

Technical Specification

510(k) Submission ID K973584
Product Code ESW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3610
Decision Date 1998-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDTRONIC INSTENT ESOPHACOIL ESOPHAGEAL STENT SYSTEM AND ESOPHACOIL EXTENSION SYSTEM received FDA 510(k) clearance under submission number K973584, sponsored by Medtech Instruments. 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 1998-01-09.

Classification & Regulation

This clearance is catalogued under FDA product code ESW and 21 CFR 878.3610, within the General, Plastic Surgery review panel as a Class II device.