FDA 510(k) Applications Submitted by A&E Medical Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K181607 06/19/2018 Thorecon Rigid Fixation System A&E Medical Corporation
K173579 11/20/2017 ThoreconÖ Fixation System A&E Medical Corporation
K193479 12/16/2019 Sternal Cable System A&E Medical Corporation


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