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# NeuroOne Medical 510(k) for Ablation System
- URL: https://www.fdaweb.com/neuroone-medical-510-k-for-ablation-system/
- Published: 2023-06-14T12:00:00.000Z
- Updated: 2026-09-14T18:38:59.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5154694

NeuroOne Medical Technologies has submitted a 510(k) for its OneRF Ablation System. The device uses already-implanted stereoelectroencephalography electrodes to record brain activity and allow for ablation of nervous tissue when connected to a proprietary radio frequency generator, NeuroOne says. The device has real-time temperature monitoring capabilities, it adds.