GARFIELD HEIGHTS, Ohio--(BUSINESS WIRE)--AxioMed® Spine Corporation (www.axiomed.com) announces the receipt of CE Mark approval for its Freedom® Cervical Disc, an elastomeric total spinal disc replacement device. The CE Mark approval was received as a result of an accredited European Notified Body conformity assessment of the Company’s complete portfolio of biocompatibility and biomechanical cervical disc testing and supporting data regarding the Freedom® technology. AxioMed’s first product was the Freedom® Lumbar Disc which received CE Mark in 2009. The CE Mark clears AxioMed for the introduction of the Freedom® Cervical Disc into the EU Market. AxioMed is an ISO 13485:2003 certified manufacturer of the Freedom Lumbar and Cervical Discs.
