Medtronic wins FDA 510(k) clearance for ProGrip Advanced mesh in robotic ventral hernia repair

Medtronic

Medtronic

MDT

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  • Medtronic filed FDA 510(k) submissions to expand its Hugo robotic-assisted surgery system into US general surgery, including hernia repair, and gynecology.
  • A separate 510(k) filing covered the LigaSure RAS Maryland instrument for use on Hugo.
  • The FDA cleared ProGrip Advanced self-gripping polypropylene mesh for robotic-assisted ventral hernia repair.


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