FDA clears Medtronic’s LigaSure RAS Maryland device

Medtronic has received clearance from the US FDA for its LigaSure RAS Maryland jaw device for use with the company’s Hugo RAS system. The Hugo RAS system is authorised for urologic surgery in the US and adopted by health systems nationwide. The LigaSure RAS Maryland instrument is designed solely for use with the Valleylab FT10 energy platform on the Hugo RAS system. Credit: Medtronic / PRNewswire. Medtronic has received clearance from the US Food and Drug Administration (FDA) for its LigaSure RAS Maryland jaw device for use with the company’s Hugo robotic-assisted surgery (RAS) system. This decision introduces Medtronic’s vessel-sealing…

Source: Medical Device Network