meddevicedb.com FDA Device Reference

ALN OPTIONAL VENA CAVA FILTER-FEMORAL APPROACH, JUGULAR APPROACH, BRACHIAL APPROACH, EXTRACTION KIT, PRECURVED EXTRACTIO

K070514 Class II Abbreviated
Decision Date
2008-01-30
Sponsor / Applicant
Aln Implants Chirurgicaux

Technical Specification

510(k) Submission ID K070514
Product Code DTK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3375
Decision Date 2008-01-30
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALN OPTIONAL VENA CAVA FILTER-FEMORAL APPROACH, JUGULAR APPROACH, BRACHIAL APPROACH, EXTRACTION KIT, PRECURVED EXTRACTIO received FDA 510(k) clearance under submission number K070514, sponsored by Aln Implants Chirurgicaux. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-01-30.

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.