FDA 510(k) Applications Submitted by TIM M LOHNES

FDA 510(k) Number	Submission Date	Device Name	Applicant
K140754	03/26/2014	COOPER SURGICAL LEISEGANG COLPOSCOPE SYSTEM	COOPER SURGICAL, INC.
K081169	04/24/2008	AUTOSUTURE VERSAPORT PLUS BLADLESS TROCAR; BLADELESS TROCAR	COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
K141123	05/01/2014	ALLIANCE SPINE RAAS CRANIAL PLATING SYSTEM	ALLIANCE PARTNERS, LLC.
K140547	03/04/2014	EXCERA FITRITE TOTAL HIP ARTHROPLASTY SYSTEM	EXCERA ORTHOPEDICS, INC.
K091016	04/09/2009	COVIDIEN SPORTS SURGERY AS MENISCAL REPAIR DEVICE WITH HIGH STRENGTH SUTURE	SURGICAL DEVICES, A GLOBAL BUSINESS UNIT COVIDIEN
K141523	06/09/2014	ALLY UPS	COOPER SURGICAL, INC.
K102291	08/12/2010	COVIDIEN ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY	COVIDIEN
K082535	09/02/2008	COVIDIEN SPORTS SURGERY AS MENISCAL REPAIR DEVICE	SURGICAL DEVICES, A GLOBAL BUSINESS UNIT COVIDIEN
K103253	11/03/2010	SILS PORT	COVIDEN (FORMERLY REGISTERED AS US SURGICAL, A DIV