FDA 510(k) Application Details - K014161

Device Classification Name	Ring, Annuloplasty   More FDA Info for this Device
510(K) Number	K014161
Device Name	Ring, Annuloplasty
Applicant	ST. JUDE MEDICAL, INC. ONE LILLEHEI PLAZA ST. PAUL, MN 55117 US Other 510(k) Applications for this Company
Contact	WILLIAM MCKELVEY Other 510(k) Applications for this Contact
Regulation Number	870.3800   More FDA Info for this Regulation Number
Classification Product Code	KRH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/19/2001
Decision Date	01/15/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review