Medtronic Seeks FDA Approval to Broaden Hugo Robotic Surgery System Use

Medtronic has filed 510(k) submissions with the FDA to expand the applications of its Hugo robotic-assisted surgery system. The company aims to include general and gynecologic surgical procedures in the United States. Additionally, Medtronic secured FDA clearance for its ProGrip™ Advanced mesh, intended for robotic-assisted ventral hernia repair.