The U.S. Food and Drug Administration has given 510(k) clearance to Amedica Corporation, SEEplate(TM) Cervical Plate system. The system incorporates features which aim at giving surgeons an alternative to the current surgical procedures that are being followed. It facilitates anterior screw fixation, thereby suiting the patient anatomy. In this way, a more consistent supplemental fixation result can be achieved for various applications such as including degenerative disc disease and spinal stenosis.