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COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM

K062264 Class II Traditional
Decision Date
2007-11-08
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K062264
Product Code FGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 2007-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEM received FDA 510(k) clearance under submission number K062264, sponsored by Medtronic Vascular. 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 2007-11-08.

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.