FDA 510(k) Application Details - K191526

Device Classification Name	Surgical Device, For Ablation Of Cardiac Tissue   More FDA Info for this Device
510(K) Number	K191526
Device Name	Surgical Device, For Ablation Of Cardiac Tissue
Applicant	Medtronic, Inc. 3800 Annapolis Lane Plymouth, MN 55447 US Other 510(k) Applications for this Company
Contact	Choua Thao Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	OCL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/10/2019
Decision Date	10/01/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
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