meddevicedb.com FDA Device Reference

ATRIUM MEDICAL CORPORATION ICAST COVERED STENT

K041269 Class II Traditional
Decision Date
2004-09-14
Sponsor / Applicant
Atrium Medical Corp.

Technical Specification

510(k) Submission ID K041269
Product Code JCT
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3720
Decision Date 2004-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ATRIUM MEDICAL CORPORATION ICAST COVERED STENT received FDA 510(k) clearance under submission number K041269, sponsored by Atrium Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2004-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code JCT and 21 CFR 878.3720, within the General, Plastic Surgery review panel as a Class II device.