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ATTUNE ADJUSTABLE FLEXIBLE ANNULOPLASTY RING MODEL AFR

K083835 Class II Special
Decision Date
2009-01-23
Sponsor / Applicant
St Jude Medical

Technical Specification

510(k) Submission ID K083835
Product Code KRH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3800
Decision Date 2009-01-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ATTUNE ADJUSTABLE FLEXIBLE ANNULOPLASTY RING MODEL AFR received FDA 510(k) clearance under submission number K083835, sponsored by St Jude Medical. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-01-23.

Classification & Regulation

This clearance is catalogued under FDA product code KRH and 21 CFR 870.3800, within the Cardiovascular review panel as a Class II device.