Medtronic the First to Offer Complete Portfolio of Full-Body MR Conditional Neurostimulation Systems for Chronic Pain
Medtronic plc
Medtronic plc

FDA Approval of Medtronic Specify® SureScan® MRI Surgical Leads Rounds Out Exclusive Portfolio Designed for Access to Full-Body MRI[*]

DUBLIN - March 3, 2016 - Medtronic plc (MDT) today announced U.S. Food and Drug Administration (FDA) approval of Specify® SureScan® MRI surgical leads, which are indicated for use as part of Medtronic implanted neurostimulation (also known as spinal cord stimulation, or SCS) systems for chronic pain. In 2013, Medtronic introduced the only implantable neurostimulation systems for use in the treatment of chronic, intractable back and/or limb pain that are FDA approved for full-body Magnetic Resonance Imaging (MRI) scans under specified conditions. The approval of SpecifySureScan MRI surgical leads establishes Medtronic as the only company with a full portfolio of SCS systems FDA approved for full-body MRI.* This means physicians can now offer a Medtronic full-body MR Conditional SCS system best suited for their patients regardless of the type of neurostimulator (rechargeable or non-rechargeable) or lead type (percutaneous or surgical). The new Specify SureScan MRI leads will be available to physicians and their patients later this month.

Studies show that 82 percent of patients implanted with a spinal cord stimulator are expected to need an MRI within five years of receiving their implant,1 and Medtronic SureScan MRI neurostimulation systems offer patients the confidence of knowing that they can receive optimal diagnostic imaging anywhere in the body should the need arise. MRI scans have become a diagnostic standard of care, allowing physicians to detect a wide range of health conditions by viewing highly detailed images of internal organs, blood vessels, muscles, joints, tumors, areas of infection and other areas of the body by using strong magnetic fields and radio frequency pulses to create images of structures inside the body. In the United States, the number of scans has nearly doubled in the past decade, with 32 million scans - more than one MRI per second -- performed in 2011.2

"All patients with a spinal cord stimulation system should have the ability to be offered the same imaging options as those without one," said Steven Falowski, M.D., neurosurgeon at St. Luke`s University Health Network in Bethlehem, Pennsylvania. "Now more than ever, patients and other health care providers are concerned about access to MRI when considering an implantable device. This approval means I can offer a neurostimulation system that helps manage my patients` pain and gives them access to the diagnostic benefits of MRI."