Cervical Arthroplasty Healthcare Professionals

PRESTIGE LP CERVICAL DISC SYSTEM

Prestige LP cervical disc implanted at 2 levels in the spine.

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 Warnings

Product Details
1

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.

2

Based on mechanical testing according to ISO (18192-1) and ASTM (F2423-05).