FDA 510(k) Applications Submitted by Matrix Surgical Holdings, LLC/Matrix Surgical USA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180249 | 01/29/2018 | OmniPore DUROMAX Surgical Implants | Matrix Surgical Holdings, LLC/Matrix Surgical USA |
| K133046 | 09/27/2013 | OMNIPORE CUSTOMIZED SURGICAL IMPLANTS | MATRIX SURGICAL HOLDINGS, LLC/MATRIX SURGICAL USA |
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