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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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