meddevicedb.com FDA Device Reference

Hilal Embolization MicroCoils

K160219 Class II Traditional
Decision Date
2016-08-03
Sponsor / Applicant
Cook Incorporated

Technical Specification

510(k) Submission ID K160219
Product Code KRD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3300
Decision Date 2016-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hilal Embolization MicroCoils received FDA 510(k) clearance under submission number K160219, sponsored by Cook Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-08-03.

Classification & Regulation

This clearance is catalogued under FDA product code KRD and 21 CFR 870.3300, within the Cardiovascular review panel as a Class II device.