Your browser is out of date
With an updated browser, you will have a better Medtronic website experience. Update my browser now.
The Prestige LP™ cervical disc is the first FDA approved one- and two-level arthroplasty device to report 10-year IDE study data. The Prestige LP titanium ceramic composite material contains no nickel, cobalt, or chromium and allows for MRI clarity of the spine. The Prestige LP uses streamlined instrumentation designed for a smooth, repeatable workflow.1,2
Indications, Safety, and WarningsProduct Details
Abkowitz, S, Abkowitz SM, Fisher H et. Al. The Development of Wear Resistant Titanium-Ceramic Composites for Orthopaedic Implant Devices. Proceedings from the Materials & Processes for Medical Devices Conference, August 25-27, 2004 St. Paul, Minnesota.
Based on mechanical testing according to ISO (18192-1) and ASTM (F2423-05).