FDA 510(k) Application Details - K143480

Device Classification Name	Catheters, Transluminal Coronary Angioplasty, Percutaneous   More FDA Info for this Device
510(K) Number	K143480
Device Name	Catheters, Transluminal Coronary Angioplasty, Percutaneous
Applicant	MEDTRONIC INC. PARKMORE BUSINESS PARK WEST GALWAY IE Other 510(k) Applications for this Company
Contact	John Kilmartin Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LOX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/08/2014
Decision Date	04/02/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review