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FDA Approves First-of-its-Kind SenSight™ Directional Lead System for DBS Therapy

(June 7, 2021) – Medtronic announced receipt of U.S. Food and Drug Administration (FDA) approval and first U.S. implants of the SenSight™ Directional Lead System for Deep Brain Stimulation (DBS) therapy. SenSight™ allows physicians to deliver precise, patient-specific DBS therapy. Click here to learn more about Medtronic and SenSight™.

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