ALTSTAETTEN, Switzerland, July 8, 2019 /PRNewswire/ — icotec AG, a Swiss company, today announced the VADER®one pedicle screw system was granted U.S. Food and Drug Administration (FDA) 510(k) clearance for both minimally-invasive and open spine surgical procedures. VADER®one, made from icotec’s unique BlackArmor® material, was designed for secure stabilization and post-operative visualization, which is important after spinal tumor procedures. Lateral …