Charles Sternberg, Associate Editor10.25.22
Medtronic has received CE Mark approval for the Hugo robotic-assisted surgery (RAS) system to be used in general surgery procedures in Europe.
The Hugo RAS system previously received CE Mark for urologic and gynaecologic procedures in October 2021. Those indications, combined with general surgery, cover about 80% of all robotic-assisted surgeries performed globally today.
Dr. Carla Peron, chief medical officer of the Surgical Robotics business in Medtronic’s Medical Surgical portfolio, shared the announcement during a podium presentation at the European Hernia Society’s annual international congress in Manchester, England.
“Robotic-assisted surgery is key to opening access to quality care and improved outcomes. The general surgery indication for Hugo is a major step in expanding the benefits of minimally invasive surgery to patients around the world,” Dr. Peron said. “Our team is looking forward to partnering with more customers to build and grow their robotic surgery programs in this hugely important area of healthcare.”
The CE Mark for general surgery spans several specialties including hernia, colorectal, and bariatric. Hernia surgery is the fourth most common operation around the world and represents the fastest-growing procedural area for robotic-assisted surgery. It is also a space where Medtronic has long had market-leading positions with its portfolio of access, dissection, mesh, and fixation products.
“Robotic-assisted surgery represents an exciting opportunity for hernia procedures, transforming the patient experience. We are thrilled to collaborate with Medtronic, our long-term partner, on this announcement and continue to shape the future of hernia treatment together,” said Dr. Filip Muysoms, president of the European Hernia Society.
Touch Surgery Enterprise is a first-of-its-kind AI-powered platform that makes sharing surgical video simple and provides surgeons with a powerful new training tool to improve performance.6 Used together, the Hugo RAS system and Touch Surgery Enterprise provide insight into procedure time, cost, and process, which has the potential to reduce burdens on healthcare systems.
The Hugo RAS system is commercially available in certain geographies. Regulatory requirements and status in individual countries and regions will determine market availability of the Hugo RAS system and approved indications. In the U.S., the Hugo RAS system is an investigational device not for sale.
References:
1 Based on internal estimates and Medtronic report, FY20 market model: procedural volume data.
2 Fitch K, Engel T, Bochner A. Cost differences between open and minimally invasive surgery. Managed Care. 2015 Sep;24(9):40–48.
3 Tiwari MM, Reynoso JF, High R, Tsang AW, Oleynikov D. Safety, efficacy, and cost effectiveness of common laparoscopic procedures. Surg Endosc. 2011;25(4):1127-1135.
4 Roumm AR, Pizzi L, Goldfarb NI, Cohn H. Minimally invasive: minimally reimbursed? An examination of six laparoscopic surgical procedures. Surg Innov. 2005;12(3):261–287.
5 Based on internal estimates and Medtronic report, FY20 market model: procedural volume data.
The Hugo RAS system previously received CE Mark for urologic and gynaecologic procedures in October 2021. Those indications, combined with general surgery, cover about 80% of all robotic-assisted surgeries performed globally today.
Dr. Carla Peron, chief medical officer of the Surgical Robotics business in Medtronic’s Medical Surgical portfolio, shared the announcement during a podium presentation at the European Hernia Society’s annual international congress in Manchester, England.
“Robotic-assisted surgery is key to opening access to quality care and improved outcomes. The general surgery indication for Hugo is a major step in expanding the benefits of minimally invasive surgery to patients around the world,” Dr. Peron said. “Our team is looking forward to partnering with more customers to build and grow their robotic surgery programs in this hugely important area of healthcare.”
Addressing Barriers to Robotic Surgery Adoption
The Hugo RAS system was designed to address barriers to robotic surgery adoption. Globally, about 4% of surgeries are performed with the assistance of a robot,1 despite offering patients the benefits of minimally invasive surgery — fewer complications, shorter hospital stays, and faster return to normal activities.2,3,4 In Western Europe, about 2% of procedures are done robotically while the majority, approximately 65%, are open surgery. The remainder are traditional minimally invasive surgery.5The CE Mark for general surgery spans several specialties including hernia, colorectal, and bariatric. Hernia surgery is the fourth most common operation around the world and represents the fastest-growing procedural area for robotic-assisted surgery. It is also a space where Medtronic has long had market-leading positions with its portfolio of access, dissection, mesh, and fixation products.
“Robotic-assisted surgery represents an exciting opportunity for hernia procedures, transforming the patient experience. We are thrilled to collaborate with Medtronic, our long-term partner, on this announcement and continue to shape the future of hernia treatment together,” said Dr. Filip Muysoms, president of the European Hernia Society.
About the Hugo RAS System
A modular, multi-quadrant platform designed for a broad range of surgical procedures, the Hugo RAS system combines wristed instruments, 3D visualization, and a cloud-based surgical video capture option in Touch Surgery Enterprise with dedicated support teams specializing in robotics program optimization, service, and training.Touch Surgery Enterprise is a first-of-its-kind AI-powered platform that makes sharing surgical video simple and provides surgeons with a powerful new training tool to improve performance.6 Used together, the Hugo RAS system and Touch Surgery Enterprise provide insight into procedure time, cost, and process, which has the potential to reduce burdens on healthcare systems.
The Hugo RAS system is commercially available in certain geographies. Regulatory requirements and status in individual countries and regions will determine market availability of the Hugo RAS system and approved indications. In the U.S., the Hugo RAS system is an investigational device not for sale.
References:
1 Based on internal estimates and Medtronic report, FY20 market model: procedural volume data.
2 Fitch K, Engel T, Bochner A. Cost differences between open and minimally invasive surgery. Managed Care. 2015 Sep;24(9):40–48.
3 Tiwari MM, Reynoso JF, High R, Tsang AW, Oleynikov D. Safety, efficacy, and cost effectiveness of common laparoscopic procedures. Surg Endosc. 2011;25(4):1127-1135.
4 Roumm AR, Pizzi L, Goldfarb NI, Cohn H. Minimally invasive: minimally reimbursed? An examination of six laparoscopic surgical procedures. Surg Innov. 2005;12(3):261–287.
5 Based on internal estimates and Medtronic report, FY20 market model: procedural volume data.