"Meditech Spine, Atlanta/USA has received the US Food and Drug Administration (FDA) 510(k) clearance to market the next generation of its Talos® line of interbody devices. These cervical intervertebral fusion devices rely on the novel implantable polymer from Invibio Biomaterial Solutions, PEEK-OPTIMA® HA Enhanced. The new material solution enables the medical device manufacturer to maintain the same design features of the existing implants."