SpineNet, LLC announces the 510(k) U.S. FDA clearance of the SpineNet SSP System. The SpineNet SSP System is an anterior cervical plate and screw system which includes fixed and variable self-tapping screws and one thru four- level plates. The implants are available in a variety of sizes to accommodate the individual anatomic and clinical circumstances of each patient.
ALPHARETTA, Ga.- SpineNet LLC, a Winter Park, Fla.-based manufacturer of spinal fusion implants, has received 510(k) clearance from the U.S. Food & Drug Administration (FDA) for its new SpineNet ACC(TM) anterior cervical cage made of Zeniva® polyetheretherketone (PEEK) rods from Solvay Specialty Polymers USA, LLC.
SpineNet, LLC announces the 510(k) U.S. FDA clearance of the SpineNet ACC System. The SpineNet ACC System is a system of wedge-shaped implants and instruments designed for anterior cervical interbody fusion. To prevent migration, the SpineNet ACC, has teeth on its superior and inferior surfaces.