Spinal Elements, a spine technology company, announced today that it has received CE mark approval for its fusion devices. The CE mark is a requirement for certain medical devices sold in the European Union. CE mark approval is a key indicator of conformance with the rigorous standards required by the Medical Device Directive and a validation of Spinal Elements’ dedication to quality, safety and compliance. The scope of the CE mark approval includes the Mosaic Stand-Alone Cervical Implant System, the Magnum Stand-Alone ALIF System, the Atomic and Sapphire Cervical Plate Systems, the Crystal Cervical Interbody System, the Mercury Classic Pedicle Screw System, and the Lucent and Lucent Magnum Lumbar Interbody Systems.
