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FDA 510(k) Applications Submitted by Aakash Jain
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120600
02/28/2012
DURAGEN SECURE DURAL REGNERATION MATRIX
INTEGRA LIFESCIENCES
K160715
03/15/2016
AccuLIF TL and PL Cage
STRYKER CORPORATION
K152651
09/16/2015
AccuLIF TL and PL Cage
STRYKER CORPORATION
K143616
12/19/2014
AccuLIF TL and PL Cage
STRYKER CORPORATION
K163591
12/20/2016
BD PosiFlush Heparin Lock Flush Syringe
Becton Dickinson and Company
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