FDA 510(k) Applications Submitted by CURTIS D TRUESDALE

FDA 510(k) Number Submission Date Device Name Applicant
K020161 01/17/2002 AGILTRAC .018 PERIPHERAL DILATATION CATHETER GUIDANT CORP.
K080143 01/22/2008 MODIFICATION TO STRYKER SPINE OASYS SYSTEM STRYKER SPINE
K100737 03/15/2010 MODIFICATION TO: TRIO+SPINAL FIXATION SYSTEM STRYKER SPINE
K080773 03/19/2008 THOR ANTERIOR PLATING SYSTEM STRYKER SPINE
K080928 04/02/2008 XIA SPINAL SYSTEM, STAINLESS STEEL UNI-PLANAR SCREWS STRYKER SPINE
K120979 04/02/2012 CAREFUSION NICOLET EDX CAREFUSION 209, INC.
K011039 04/05/2001 OMNILINK .018 BILIARY STENT SYSTEM GUIDANT CORP.
K101144 04/23/2010 MODIFICATION TO:RADIUS SPINAL SYSTEM STRYKER SPINE
K091291 05/01/2009 XIA 3 SPINAL SYSTEM, UNIPLANNER/REDUCTION SCREWS & VITALLIUM ROD STRYKER SPINE
K011506 05/16/2001 OMNILINK .035 BILIARY STENT SYSTEM GUIDANT CORP.
K141719 06/25/2014 BIOGEL PL MICRO SURGICAL GLOVE MOLNLYCKE HEALTH CARE, US LLC
K102235 08/09/2010 MANTIS SPINAL SYSTEM & MANTIS REDUX SPINAL SYSTEM STRYKER SPINE
K092605 08/24/2009 XIA 4.5 SPINAL SYSTEM STRYKER SPINE
K082608 09/08/2008 RADIUS SPINAL SYSTEM, VITALLIUM ROD #486613601 STRYKER SPINE
K073151 11/08/2007 MANTIS SPINAL SYSTEM STRYKER CORP.
K103292 11/08/2010 TRIO TRAUMA SPINAL SYSTEM STRYKER CORPORATION
K083393 11/17/2008 XIA 3 SPINAL SYSTEM STRYKER SPINE
K073437 12/06/2007 THOR ANTERIOR PLATING SYSTEM STRYKER SPINE
K140477 02/26/2014 BIOGEL PS SURGICAL GLOVE SERIES, BIOGEL SKINSENSE SURGICAL GLOVE SERIES MOLNLYCKE HEALTH CARE US, LLC
K132048 07/02/2013 BARRIER EASYWARM ACTIVE SELF-WARMING BLANKET MOLNLYCKE HEALTH CARE US, LLC
K092631 08/26/2009 MANTIS REDUX SPINAL SYSTEM STRYKER SPINE


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