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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