FDA 510(k) Applications Submitted by Burt Goodson

FDA 510(k) Number	Submission Date	Device Name	Applicant
K140036	01/07/2014	APTUS HELI-FX GUIDE - 22CM DEFLECTABLE LENGTH; APTUS HELI-FX GUIDE - 28CM DEFLECTABLE LENGTH; APTUS HELI-FX APPLIER WITH	APTUS ENDOSYSTEMS, INC.
K130677	03/13/2013	APTUS HELI-FX AORTIC SECUREMENT SYSTEM	APTUS ENDOSYSTEMS, INC.
K121168	04/17/2012	APTUS 18FR HELIFX GUIDE-22 DEFLECTABLE LENGTH	APTUS ENDOSYSTEMS, INC.
K141041	04/23/2014	APTUS HELI-FX ANCILLARY ENDOANCHOR CASSETTE	APTUS ENDOSYSTEMS
K171427	05/15/2017	Heli-FX Applier, Heli-FX Guide, Ancillary EndoAnchor Cassette	Medtronic Vascular, Inc.
DEN100026	12/14/2010	APTUS STEERABLE ENDOGUIDE WITH OBTURATOR, APTUS ENDOSTAPLE APPLIER WITH ENDOSTAPLE CASSETTE, APTUS ENDOSTAPLE CASSETTE	APTUS ENDOSYSTEMS, INC.