VOL. 129 | NO. 145 | Monday, July 28, 2014
Medtronic Wins Approval For Cervical Disc Product
By Don Wade
Medtronic, Inc. has received approval from the U.S. Food and Drug Administration to market the Prestige LP Cervical Disc System for the treatment of single-level cervical disc disease (radiculopathy and/or myelopathy).
The Prestige LP Cervical Disc is the third clinically proven artificial cervical disc in the Medtronic portfolio and builds upon the same design principles as the original Prestige Cervical Disc introduced in 2007.
Instead of utilizing bone screws to attach to the vertebral bodies as in the original Prestige design, the LP design incorporates two rails positioned off midline that press-fit into two pre-drilled holes created during the surgical procedure. In addition, the Prestige LP Disc is composed of a proprietary titanium-ceramic composite that has been shown to have a lower wear rate and produce less scatter on postoperative magnetic resonance imaging (MRI) than stainless steel (MR Conditional at 3 Tesla).
“Our goal was to maintain the same ball-and-trough articulation as in the original design, but to find a way to decrease the profile and use a material with improved postoperative MRI visualization,” said Dr. Vincent Traynelis, director of Neurosurgery Spine Services and vice chairperson and professor of the Department of Neurosurgery at Rush University Medical Center in Chicago. “To address these issues, the Prestige LP Disc incorporates a dual-rail fixation mechanism instead of bone screws and is made of a titanium-ceramic composite instead of stainless steel.”
The Prestige LP Cervical Disc has been available outside the United States since 2004 and has been studied in a prospective, multicenter, historical-controlled U.S. IDE trial for a single-level indication, according to Medtronic.