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FDA 510(k) Applications Submitted by Christopher J. Medberry
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160167
01/27/2016
DePuy Synthes TFNA Augmentation System
Synthes (USA) Products, LLC
K170802
03/17/2017
TRAUMACEMÖ V+ Injectable Bone Cement
Synthes (USA) Products, LLC
K180821
03/30/2018
TruMatch Graft Cage - Long Bone
Synthes (USA) LLC
K162124
08/01/2016
Synthes 4.5mm VA-LCP Curved Condylar Plate System Line Extension, Variable Angle Positioning Pins
DePuy Synthes
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