FDA 510(k) Application Details - K220568

Device Classification Name	Catheter, Peripheral, Atherectomy   More FDA Info for this Device
510(K) Number	K220568
Device Name	Catheter, Peripheral, Atherectomy
Applicant	Cardiovascualr Systems Inc. 1225 Old Highway 8 NW New Brighton, MN 55112 US Other 510(k) Applications for this Company
Contact	Kris Miller Other 510(k) Applications for this Contact
Regulation Number	870.4875   More FDA Info for this Regulation Number
Classification Product Code	MCW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/28/2022
Decision Date	04/27/2022
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