FDA 510(k) Applications Submitted by Charles Horrell
| 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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