FDA 510(k) Applications Submitted by Brian Young

FDA 510(k) Number	Submission Date	Device Name	Applicant
K030311	01/30/2003	HEM-O-LOK XL CLIP	WECK
K170411	02/10/2017	ER-REBOA Catheter	Prytime Medical Devices, Inc
K200459	02/25/2020	pREBOA-PRO Catheter	Prytime Medical Devices, Inc.
K011660	05/29/2001	WECK CARDIAC PACING WIRES	WECK CLOSURE SYSTEMS
K982313	07/01/1998	HORIZON TITANIUM CLIPS, HORIZON TANTALUM CLIPS	WECK CLOSURE SYSTEMS
K061939	07/10/2006	MODIFICATION TO ALLOMATRIX CUSTOM	WRIGHT MEDICAL TECHNOLOGY, INC.
K172790	09/15/2017	ER-REBOA Catheter	Prytime Medical Devices, Inc.
K993157	09/21/1999	HEM-O-LOK SMX POLYMER CLIPS, MODEL 544220, HEM-0-LOK MLX POLYMER CLIPS, MODEL 544240	WECK CLOSURE SYSTEMS
K133232	10/21/2013	PREVENA INCISION MANAGEMENT SYSTEM WITH CUSTOMIZABLE DRESSING, PREVENA INCISION MANAGEMANT SYSTEM WITH PEEL& PLACE DRES	KCI USA, INC. (KINETIC CONCEPTS, INC.)
K003337	10/25/2000	HEM-O-LOK SMX, MODEL 544220; HEM-O-LOK ML, MODEL 544230; HEM-O-LOK MLX, MODEL 544240	WECK CLOSURE SYSTEMS
K053319	11/30/2005	ALLOMATRIX CUSTOM	WRIGHT MEDICAL TECHNOLOGY, INC.
K193440	12/11/2019	ER-REBOA PLUS Catheter	Prytime Medical Devices, Inc
K060011	01/03/2006	MIIG SR	WRIGHT MEDICAL TECHNOLOGY, INC.
K041663	06/18/2004	ALLOMATRIX TCP, ALLOMATRIX W/CASO4 FILLED TCP, AND ALLOMATRIX PLUS CBM	WRIGHT MEDICAL TECHNOLOGY, INC.
K982944	08/21/1998	HEM-O-LOCK, MODEL 523935	WECK CLOSURE SYSTEMS