FDA 510(k) Applications Submitted by KRISTEN MEANY, MS, CQA, RAC

FDA 510(k) Number Submission Date Device Name Applicant
K141217 05/12/2014 ACCULIF TL AND PL CAGE STRYKER CORPORATION
K112534 09/01/2011 LIFECELL TISSUE EXPANDER LIFECELL CORP.
K142699 09/22/2014 LITe Plate System STRYKER CORPORATION
K132968 09/23/2013 UNIVISE SPINOUS PROCESS FIXATION PLATE (35MM, 40MM) STRYKER SPINE


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