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FDA 510(k) Applications Submitted by Akros Medical
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200361
02/14/2020
Akros Scruture Anchor LisFranc Repair Kit
Akros Medical
K162805
10/05/2016
Akros Fibulink Syndesmosis Repair Kit
Akros Medical
K173550
11/16/2017
Akros FibuLinkÖ Syndesmosis Repair Kit
Akros Medical
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