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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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