Medtronic gets FDA approval for BrainSense device in Parkinson's patients
15 Articles
15 Articles
In Parkinson’s fight, Medtronic’s first-in-the-world adaptive therapy feature wins FDA approval
After decades of development and trials, Medtronic has secured U.S. Food and Drug Administration approval for adaptive technology personalizing treatment of Parkinson’s symptoms using advanced stimulation deep in the brain. On Monday, the Fridley-run company announced the regulatory win for its BrainSense Adaptive deep brain stimulation in a thin, surgically-implanted neurostimulator in the chest with leads stretching through the neck to the bra…
FDA Approves Adaptive Deep Brain Stimulator for Parkinson's Disease
(MedPage Today) -- The FDA approved adaptive deep brain stimulation (DBS) technology (BrainSense adaptive DBS and BrainSense electrode identifier) for people with Parkinson's disease, Medtronic announced Monday. Like other DBS devices, the newly...
Parkinson’s Patients Now Have a New Way to Manage Symptoms
There is still no cure for Parkinson’s disease, but the U.S. Food and Drug Administration (FDA) approved a new deep brain stimulator that could benefit patients with the motor condition. On Feb 24, the FDA approved Medtronic’s BrainSense Adaptive deep brain stimulation, a device that surgeons implant in patients’ chests with electrodes connecting to the brain. The system is programmed to respond to and manage abnormal brain signals that contribu…
FDA Approves Personalized Brain Stimulation Device for Parkinson’s
Medtronic has announced FDA approval of BrainSense Adaptive deep brain stimulation (aDBS) and BrainSense Electrode Identifier (EI) for patients with Parkinson’s. “Medtronic is the only company in the world to offer an adaptive DBS system that dynamically adjusts therapy in real time,” said Brett Wall, executive vice president and president of the Medtronic Neuroscience Portfolio. He added, “This new era in Parkinson’s care represents more than a…
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