FDA 510(k) Application Details - K200117

Device Classification Name	More FDA Info for this Device
510(K) Number	K200117
Device Name	Trevo NXT ProVue Retriever
Applicant	Stryker 47900 Bayside Parkway Fremont, CA 94538 US Other 510(k) Applications for this Company
Contact	Germaine Fu 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	01/21/2020
Decision Date	02/07/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review