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FDA 510(k) Applications Submitted by TIM 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
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