meddevicedb.com FDA Device Reference

COOK CELECT PLATINUM VENA CAVA FILTER SET FOR FEMORAL APPROACH COOK CELECT PLATIUM VENA CAVA FILTER SET FOR JUGULAR APPR

K121629 Class II Traditional
Decision Date
2012-07-03
Sponsor / Applicant
William Cook Europe Aps

Technical Specification

510(k) Submission ID K121629
Product Code DTK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3375
Decision Date 2012-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COOK CELECT PLATINUM VENA CAVA FILTER SET FOR FEMORAL APPROACH COOK CELECT PLATIUM VENA CAVA FILTER SET FOR JUGULAR APPR received FDA 510(k) clearance under submission number K121629, sponsored by William Cook Europe Aps. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-07-03.

Classification & Regulation

This clearance is catalogued under FDA product code DTK and 21 CFR 870.3375, within the Cardiovascular review panel as a Class II device.