Spes Medica Srl FDA Approvals

0 new drug approvals and 2 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Subdural Electrode, Strip/Intraoperative Strip, Grid/Intraoperative Grid, Multi-Strip and Split Grid, Intraoperative Mapping Grid510(k)Nov 10, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Nov 10, 2022
AC Cream - Conductive paste510(k)Dec 1, 2021Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Dec 1, 2021