FDA 510(k) Applications Submitted by Jeffrey Krawiec

FDA 510(k) Number Submission Date Device Name Applicant
K180310 02/05/2018 DePuy Synthes Trauma Orthopedic Plates and Screws Synthes (USA) Products LLC/DePuy Orthopaedics Inc
K190963 04/12/2019 DePuy Synthes Craniomaxillofacial Sternal Devices - MR Conditional Synthes (USA) Products LLC
K192702 09/27/2019 DePuy Synthes Craniomaxillofacial Neuro Devices - MR Conditional Synthes (USA) Products LLC


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