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X-SIZER CATHETER SYSTEM

K021096 Class II Traditional
Decision Date
2004-09-08
Sponsor / Applicant
Ev3 Corporation

Technical Specification

510(k) Submission ID K021096
Product Code MCW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4875
Decision Date 2004-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-SIZER CATHETER SYSTEM received FDA 510(k) clearance under submission number K021096, sponsored by Ev3 Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code MCW and 21 CFR 870.4875, within the Cardiovascular review panel as a Class II device.