Us Fda Grants Breakthrough Device Designation To Explore Use Of Abbotts Deep Brain Stimulation System To Manage Severe Depression
Abbott Announced That The Us Food And Drug Administration (Fda) Has Granted Breakthrough Device Designation To Investigate The Use Of Its Deep Brain Stimulation (Dbs) System In Treatment-Resistant Depression (Trd), A Form Of Major Depressive Disorder (Mdd). Breakthrough Device Designation Expedites The Review Of Innovative Technologies That Can Improve The Lives Of People With Life-Threatening Or Irreversibly Debilitating Diseases Or Conditions.Abbott'S Dbs System Is A Personalized, Adjustable Therapy That Involves Implanting Thin Wires
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