Die CorTec GmbH gab heute bekannt, dass die US-amerikanische Food and Drug Administration (FDA) das Unternehmen in ihr Total Product Life Cycle Advisory Program (TAP) aufgenommen hat. Mit der TAP-Aufnahme wird das Brain Interchange™ BCI-System als vorrangige Innovation für die motorische Rehabilitation nach Schlaganfall eingestuft. Die Aufnahme folgt auf die kürzlich erteilte FDA Breakthrough Device Designation. CorTec zählt damit zu den wenigen Neurotech-Unternehmen weltweit, die beide Anerkennungen erhalten haben. Zudem wurde im Rahmen der laufenden, von den NIH finanzierten und der FDA genehmigten klinischen Studie ein dritter Patient am Harborview Medical Center in Seattle erfolgreich implantiert. Die Studie wird von
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