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FDA 510(k) Applications Submitted by Rebecca Reiter
FDA 510(k) Number
Submission Date
Device Name
Applicant
K183113
11/09/2018
DePuy Synthes Maxillofacial Portfolio - MR Conditional
Synthes (USA) Products LLC
K131186
04/25/2013
SYNTHES 2.7MM AND 3.5MM VARIABLE ANGLE LCP MIDFOOT/HINDFOOT SYSTEM
SYNTHES (USA) PRODUCTS LLC
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