The product was first introduced outside the US in November 2004 and has now been used to treat over 7,500 patients worldwide, including those involved in this 2-arm IDE study. The controlled mobility of the Mobi-C’s insert is designed to restore and respect the instantaneous axes of rotation for a return to physiological mobility of the intervertebral disc and the cervical spine. This innovative mobile bearing design reduces the stresses on the bone-implant interface, eliminating the need for invasive vertebral anchorage such as screws or keels and allowing for multi-level use.

Christophe Lavigne, president and CEO of LDR says, “Completion of the 24-month follow-up phase of our one-level study represents another giant milestone for our company that will bring us closer to our goal of becoming the first and only metal-on-polyethylene one-level and two-level cervical disc to obtain FDA approval. We believe that the unique benefits of Mobi-C will establish it as the gold standard for cervical disc arthroplasty in the United States as it is outside the U.S. We are proud to have achieved this milestone at the same time that we are experiencing tremendous success with our VerteBRIDGE™ plating technology in the zero-profile ROI-A™ lumbar and ROI-C™ cervical cages. We are looking forward to a continued focus on bringing innovative products to our surgeon customers.”