meddevicedb.com FDA Device Reference

WALLFLEX PARTIALLY COVERED ESOPHAGEAL STENT SYSTEM

K073266 Class II Traditional
Decision Date
2008-02-27
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K073266
Product Code ESW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3610
Decision Date 2008-02-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WALLFLEX PARTIALLY COVERED ESOPHAGEAL STENT SYSTEM received FDA 510(k) clearance under submission number K073266, sponsored by Boston Scientific Corp. 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 2008-02-27.

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.