GMReis receives FDA 510 (k) approval to market PEDIMAX II - PEDICULAR SCREW SYSTEM in the USA Posted on 1 de February de 20192 de June de 2022 by admin On February 1, 2019, GMReis received the # FDA510 (k) clearance for the product “Pedimax II – Pedicular Screw Spinal System” and can be consulted by registration K180626.