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FDA 510(k) Applications Submitted by KRISTEN MEANY
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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