FDA 510(k) Application Details - K172359

Device Classification Name	More FDA Info for this Device
510(K) Number	K172359
Device Name	UroLift System (UL500)
Applicant	NeoTract, Inc. 4473 Willow Road Suite 100 Pleasanton, CA 94588 US Other 510(k) Applications for this Company
Contact	Louis-Pierre Marcoux Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PEW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/04/2017
Decision Date	08/18/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review