Boston Scientific's (BSX) Vercise Gevia DBS Gets FDA Nod

 | Aug 19, 2019 09:03PM ET

Boston Scientific Corporation (NYSE:BSX) recently received FDA approval for its ImageReady MRI labeling for the Vercise Gevia Deep Brain Stimulation (DBS) system. The system, to be used in a full-body magnetic resonance imaging (MRI) environment, strengthens Boston Scientific’s neuromodulation portfolio.

The Vercise Gevia DBS system, along with the Vercise Cartesia Directional Lead, is designed to treat symptoms of Parkinson's Disease (PD) by delivering targeted electrical stimulation in the brain to provide maximum relief arising from the symptoms and control the unwanted side effects in an optimal way.

More Details on PD

PD is a progressive nervous system disorder that affects movement. The symptoms start gradually, sometimes with a barely noticeable tremor in one hand. Other symptoms might include shaking, muscle stiffness and slow movement.

Significance of the Approval

Boston Scientific believes that the Vercise Gevia DBS therapy will help patients with PD control symptoms, leading to an improved quality of life. The system will perform a full-body MRI of patients, who will receive benefits from the latest advancements in the DBS program like directional stimulation and a longer-lasting rechargeable battery.