FDA 510(k) Applications Submitted by Rhoda M. Santos

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120850	03/21/2012	TARGET DETACHABLE COIL	STRYKER NEUROVASCULAR
K131492	05/23/2013	MODIFIED FLOWGATE BALLOON GUIDE CATHETER	CONCENTRIC MEDICAL, INC.
K192122	08/06/2019	Trevo Trak 21 Microcatheter	Stryker
K133177	10/17/2013	MODIFIED HD GUIDE CATHETER	CONCENTRIC MEDICAL, INC.
K123377	11/01/2012	TARGET DETACHABLE COIL	STRYKER NEUROVASCULAR
K113412	11/18/2011	TARGET DETACHABLE COIL	STRYKER NEUROVASCULAR
K151667	06/19/2015	AXS Catalyst Distal Access Catheter 058x115cm, AXS Catalyst Distal Access Catheter 058x132cm, AXS Catalyst Distal Access Catheter 060x132cm	Stryker
K192207	08/14/2019	Trevo NXT ProVue Retriever	Stryker
K103355	11/16/2010	GDC 360 DETEACHABLE COIL	BOSTON SCIENTIFIC CORP.
K150616	03/10/2015	Trevo XP ProVue Retriever (4x30mm)	Concentric Medical, Inc.
K190779	03/27/2019	Trevo XP ProVue Retriever	Stryker
K173352	10/25/2017	Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)	Concentric Medical, Inc.