FDA 510(k) Application Details - K190779

Device Classification Name	More FDA Info for this Device
510(K) Number	K190779
Device Name	Trevo XP ProVue Retriever
Applicant	Stryker 47900 Bayside Parkway Fremont, CA 94538 US Other 510(k) Applications for this Company
Contact	Rhoda M. Santos Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	POL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/27/2019
Decision Date	06/25/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review