meddevicedb.com FDA Device Reference

BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM

K011080 Class II Traditional
Decision Date
2001-10-11
Sponsor / Applicant
Medtronic Ave, Inc.

Technical Specification

510(k) Submission ID K011080
Product Code FGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 2001-10-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRIDGE SE SELF-EXPANDING STENT DELIVERY SYSTEM received FDA 510(k) clearance under submission number K011080, sponsored by Medtronic Ave, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2001-10-11.

Classification & Regulation

This clearance is catalogued under FDA product code FGE and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.