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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.
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