FDA 510(k) Application Details - K173734

Device Classification Name	Stent, Ureteral   More FDA Info for this Device
510(K) Number	K173734
Device Name	Stent, Ureteral
Applicant	Promepla SAM 9 Avenue Albert II Monaco 98000 MC Other 510(k) Applications for this Company
Contact	Alexandre Bareille Other 510(k) Applications for this Contact
Regulation Number	876.4620   More FDA Info for this Regulation Number
Classification Product Code	FAD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/06/2017
Decision Date	03/12/2018
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review