meddevicedb.com FDA Device Reference

Expro Elite Snare, Sympro Elite Snare

K163307 Class II Traditional
Decision Date
2017-03-08
Sponsor / Applicant
Vascular Solutions, Inc.

Technical Specification

510(k) Submission ID K163307
Product Code MMX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2017-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Expro Elite Snare, Sympro Elite Snare received FDA 510(k) clearance under submission number K163307, sponsored by Vascular Solutions, 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 2017-03-08.

Classification & Regulation

This clearance is catalogued under FDA product code MMX and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.