Centinel Spine Receives MDR Certification for prodisc® C Vivo and prodisc® C Nova Cervical Disc Systems

Centinel Spine has announced that its prodisc® C Vivo and prodisc® C Nova Cervical Total Disc Replacement (TDR) systems have received CE marking and certification under the EU Medical Device Regulation (MDR). This certification confirms the devices meet the highest European standards for safety, quality, and performance.

The prodisc C Vivo and prodisc C Nova systems, which have been clinically used worldwide since 2009, are among the most frequently employed cervical TDR systems globally. The devices have now been certified to comply with MDR, a challenging and rigorous process that ensures the highest level of care and patient safety.

Centinel Spine CEO Steve Murray highlighted the significance of this achievement, noting it demonstrates the company’s commitment to providing high-quality, clinically-proven products. The prodisc devices incorporate prodisc CORE technology, which has led to over 275,000 successful implantations globally. The MDR certification ensures continued access to these advanced technologies for European surgeons, helping to improve patient outcomes in cervical spine surgery.