meddevicedb.com FDA Device Reference

6248VAL ADJUSTABLE VALVE

K052459 Class II Traditional
Decision Date
2006-01-11
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K052459
Product Code DTL
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4290
Decision Date 2006-01-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

6248VAL ADJUSTABLE VALVE received FDA 510(k) clearance under submission number K052459, sponsored by Medtronic Vascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-01-11.

Classification & Regulation

This clearance is catalogued under FDA product code DTL and 21 CFR 870.4290, within the Cardiovascular review panel as a Class II device.