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ABSOLUTE .035 SELF-EXPANDING BILIARY STENT SYSTEM

K033393 Class II Special
Decision Date
2003-11-10
Sponsor / Applicant
Guidant Corp.

Technical Specification

510(k) Submission ID K033393
Product Code FGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 2003-11-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABSOLUTE .035 SELF-EXPANDING BILIARY STENT SYSTEM received FDA 510(k) clearance under submission number K033393, sponsored by Guidant Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2003-11-10.

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.