FDA 510(k) Applications Submitted by ROBERT BURDEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K143547 | 12/15/2014 | Vivorte Trabexus EB | VIVORTE, INC |
| K143549 | 12/15/2014 | Vivorte Trabexus | VIVORTE, INC |
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