Parkinson's disease patients and advocates are marking Friday as the start of a new era for treatment of the illness as a ...

Medtronic has received CE marks under the European Union’s Medical Device Regulation (EU MDR) for the BrainSense adaptive deep brain stimulation (aDBS) system and electrode identifier (EI ...

Adding to its Activa line of deep brain stimulation (DBS) devices, Medtronic has announced the US and European launch of its new Activa SC DBS system. The new implant is a single-channel ...

Stanford University School of Medicine neurologist Helen Bronte-Stewart is shown working with a Parkinson's disease patient during clinical trials of a new device to control tremors and other ...

Continued FDA device monitoring has resulted in fewer reports of EMI with the DBS than for spinal stimulators (SS). Although the product label information from Medtronic includes internal ...

Medtronic has recalled embolization devices collectively linked to reports of 17 injuries and four deaths, the Food and Drug Administration said Tuesday. The recall has two elements: Medtronic is ...

The personalized approach aims to reduce side effects as well as the need for device reprogrammings ... follows up on Medtronic’s CE mark for adaptive deep-brain stimulation, which was obtained ...

Medtronic has recalled certain Pipeline Vantage Embolization Devices with Shield Technology due to an increased risk of incomplete wall apposition and braid deformation, which could lead to stroke ...

Former top lawyers at major companies decry Trump orders against law firms Former top legal executives at large companies including Microsoft , Intel and Eli Lilly submitted a legal brief on ...