FDA 510(k) Application Details - K150452

Device Classification Name	Catheter, Angioplasty, Peripheral, Transluminal   More FDA Info for this Device
510(K) Number	K150452
Device Name	Catheter, Angioplasty, Peripheral, Transluminal
Applicant	Summa Therapeutics, LLC 257 Castro Street, #216 Mountain View, CA 94041 US Other 510(k) Applications for this Company
Contact	Richard Rush Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	LIT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/20/2015
Decision Date	08/13/2015
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