meddevicedb.com FDA Device Reference

TrailBlazer Angled Support Catheter

K162384 Class II Traditional
Decision Date
2016-09-22
Sponsor / Applicant
Medtronic Vascular, Inc.(Formerly Ev3 Inc.)

Technical Specification

510(k) Submission ID K162384
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2016-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TrailBlazer Angled Support Catheter received FDA 510(k) clearance under submission number K162384, sponsored by Medtronic Vascular, Inc.(Formerly Ev3 Inc.). The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.