FDA 510(k) Applications Submitted by Spes Medica SRL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K211954 | 06/23/2021 | Subdural Electrode, Strip/Intraoperative Strip, Grid/Intraoperative Grid, Multi-Strip and Split Grid, Intraoperative Mapping Grid | Spes Medica SRL |
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