FDA 510(k) Application Details - K172033

Device Classification Name	Catheter, Angioplasty, Peripheral, Transluminal   More FDA Info for this Device
510(K) Number	K172033
Device Name	Catheter, Angioplasty, Peripheral, Transluminal
Applicant	ArraVasc Ltd 2 Ballybrit Business Park Galway h91dt7c IE Other 510(k) Applications for this Company
Contact	Carmel Doherty 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	07/05/2017
Decision Date	08/31/2017
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