Medtronic Brain Device Receives European Approval

Medtronic has announced that it has received the European CE Mark of regulatory approval to use its deep brain stimulation therapy to control seizures in some epilepsy patients.

Advertisement

The implantable pacemaker-like device will be introduced to hospitals throughout Europe by the end of the year, but the U.S. timeline is unclear. The FDA is reviewing Medtronic’s application to broaden use of the device, according to the report.

Read the news release on the approval of the brain device from Medtronic.

Read more coverage on orthopedic and spine devices:

10 Orthopedic and Spine Devices Recently Launched or Approved

Electronic Spinal Devices to Treat Back Pain Now Used on a Wider Array of Patients

At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.

Advertisement

Next Up in Spinal Tech

Advertisement

Comments are closed.