FDA 510(k) Applications Submitted by DAVID D COX

FDA 510(k) Number	Submission Date	Device Name	Applicant
K070238	01/25/2007	AMPLATZER RELIANT CATHETER DELIVERY SYSTEM	AGA MEDICAL CORP.
K060400	02/15/2006	CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 68000; CARDIOBLATE BP2 SURGICAL ABLATION DEVICE, MODEL 60831; CARDIOBLAT	MEDTRONIC INC.
K081082	04/16/2008	U-CLIP UNI-FIRE, MODEL M65	MEDTRONIC INC.
K062057	07/20/2006	U-CLIP DEVICE, MODEL NC65	MEDTRONIC VASCULAR
K053252	11/21/2005	U-CLIP DEVICE, MODELS B140, B160 AND B180	MEDTRONIC VASCULAR
K043291	11/29/2004	CARDIOBLATE DISPERSIVE ELECTRODE ADAPTER (ACCESSORY), MODEL 60884	MEDTRONIC VASCULAR
K153690	12/23/2015	PriMatrix Dermal Repair Scaffold	TEI BioSciences Inc.