FDA 510(k) Applications Submitted by Matthew MacEwan
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161278 | 05/06/2016 | Cerafix Dura Substitute | ACERA SURGICAL, INC. |
| K172603 | 08/30/2017 | Cerafix Dura Substitute | Acera Surgical, Inc. |
| K153613 | 12/17/2015 | Cerafix Dura Substitute | ACERA SURGICAL, INC. |
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