meddevicedb.com FDA Device Reference

ADVANIX DOUBLE PIGTAIL BILIARY STENT

K101786 Class II Special
Decision Date
2010-07-23
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K101786
Product Code FGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 2010-07-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANIX DOUBLE PIGTAIL BILIARY STENT received FDA 510(k) clearance under submission number K101786, sponsored by Boston Scientific 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 2010-07-23.

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.