August: Medtronic received CE Mark approval for its latest spinal cord stimulator. Mainstay Medical completed enrollment for its randomized clinical trial for its ReActiv8 restorative neurostimulation ...

The Food and Drug Administration on Tuesday classified Medtronic’s recall of its Pipeline Vantage embolization devices as the most serious type of recall. The recall removed Pipeline Vantage 027 ...

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 ...

FDA Classifies Recall of Medtronic Embolization Devices as 'Most Serious' (Reuters) -The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as ...

Researchers at NeuroRestore, led by Grégoire Courtine and Jocelyne Bloch, have developed a technology that combines rehabilitation robotics with an implanted spinal cord neuroprosthesis. Integrating ...

The Pipeline Vantage embolization device. [Image courtesy of Medtronic] The FDA deemed a recall of some Medtronic (NYSE: MDT) + Pipeline Vantage embolization devices serious after multiple deaths ...

US shipbuilding problems are decades old and raising concerns about US Navy readiness. Officials, naval affairs experts, and politicians believe the primary issue revolves around workers.

But this approach carries fundamental problems that could doom the plan to failure before it is even implemented. The Israeli prime minister has been clear in his opposition to any role for the PA ...

The tech should improve recovery outcomes. In 2022, New Atlas reported on how an implanted spinal cord stimulator had enabled nine patients, paralyzed following a spinal cord injury, to walk.

Please provide your email address to receive an email when new articles are posted on . Spinal cord stimulation offers relief for patients who have not responded to other treatments for chronic ...