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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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