meddevicedb.com FDA Device Reference

MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01

K022420 Class II Traditional
Decision Date
2002-10-22
Sponsor / Applicant
Micrus Corp.

Technical Specification

510(k) Submission ID K022420
Product Code HCG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5950
Decision Date 2002-10-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01 received FDA 510(k) clearance under submission number K022420, sponsored by Micrus Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2002-10-22.

Classification & Regulation

This clearance is catalogued under FDA product code HCG and 21 CFR 882.5950, within the Neurology review panel as a Class II device.