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WALLSTENT ESOPHAGEAL PROSTHESIS

K940395 Class II Traditional
Decision Date
1994-09-20
Sponsor / Applicant
Boston Scientific Scimed, Inc.

Technical Specification

510(k) Submission ID K940395
Product Code ESW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3610
Decision Date 1994-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WALLSTENT ESOPHAGEAL PROSTHESIS received FDA 510(k) clearance under submission number K940395, sponsored by Boston Scientific Scimed, Inc.. 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 1994-09-20.

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.