NeuroPace submits safety, effectiveness data from RNS System study to FDA

NeuroPace (NPCE) announced FDA submission of three-year safety and effectiveness data from its prospective post-approval study of the RNS System in adults with drug-resistant focal epilepsy. The study enrolled more than three hundred patients from more than thirty leading Level 4 Comprehensive Epilepsy Centers in the United States, making it the largest prospectively enrolled trial in the field of neuromodulation for drug-resistant focal epilepsy.