FDA 510(k) Applications Submitted by SHARON ALEXANDER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K080898	03/31/2008	AUTO SUTURE ENDO GIA STAPLERS WITH ENDO GIA SINGLE USE LOADING UNITS WITH STAPLE LINE REINFORCEMENT	TYCO HEALTHCARE GROUP, LP
K081050	04/14/2008	PARIETEX PROGRIP MESH	SOFRADIM PRODUCTION
K081126	04/21/2008	PARIETEX COMPOSITE MONO PM MESH	SOFRADIM PRODUCTION
K101197	04/28/2010	PARIE TENE PROGRIP MESH	SOFRADIM PRODUCTION
K123156	10/09/2012	GORE FLOW REVERSAL SYSTEM MODEL GFRS073	W. L. GORE & ASSOCIATES, INC.
K072951	10/18/2007	PARIETENE DUO AND QUADRA POLYPROPYLENE MESHES	SOFRADIM PRODUCTION
K073164	11/09/2007	IVS TUNNELLER DEVICES	COVIDIEN UK MANUFACTURING LTD
K073287	11/21/2007	PREVADH MESH	SOFRADIM PRODUCTION