meddevicedb.com FDA Device Reference

HYPERGLIDE AND HYPERFORM OCCLUSION BALLOON SYSTEMS

K101570 Class II Traditional
Decision Date
2010-07-13
Sponsor / Applicant
Micro Therapeutics Dba Ev3 Neurovascular

Technical Specification

510(k) Submission ID K101570
Product Code MJN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4450
Decision Date 2010-07-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYPERGLIDE AND HYPERFORM OCCLUSION BALLOON SYSTEMS received FDA 510(k) clearance under submission number K101570, sponsored by Micro Therapeutics Dba Ev3 Neurovascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-07-13.

Classification & Regulation

This clearance is catalogued under FDA product code MJN and 21 CFR 870.4450, within the Cardiovascular review panel as a Class II device.