TSolution One robot for total knee replacement receives FDA approval

The Robot Report

FREMONT, Calif. — Think Surgical Inc. this week announced that the U.S. Food and Drug Administration has granted clearance for it to market the TSolution One system for total knee replacement in the U.S. The robot already has CE Marking, and surgeons have used it in more than 550 procedures in the Asia-Pacific and European markets.

“We are thrilled to expand the use of this state-of-the-art technology, which is truly transforming orthopedic surgery,” stated John Hahn, CEO and president of Think Surgical. “FDA clearance of TSolution One furthers our commitment to improving the lives of patients suffering from severe osteoarthritis by expanding the global commercialization of our active robot for TKA [total knee arthroplasty].”

In March, Think Surgical raised $134 million in funding. It joins Stryker Corp.‘s Mako system, Smith & Nephew PLC’s Navio, and several other companies in the competitive orthopedic market.

TSolution One technology and trials

The TSolution One total knee application includes CT-based, 3D pre-surgical planning software that enables a surgeon to prepare, in a virtual environment, the patient’s unique joint-replacement plan using a number of implant options.

During total knee replacement surgery, the surgeon implements the patient’s preplanned procedure using the robot, which prepares the joint according to the surgeon’s plan for precise placement of implants.


The Robot Report is launching the Healthcare Robotics Engineering Forum, which will be on Dec. 9-10 in Santa Clara, Calif. The conference and expo will focus on improving the design, development, and manufacture of next-generation healthcare robots. Learn more about the Healthcare Robotics Engineering Forum, and registration is now open.


Five surgeons participated in the clinical trial, which confirmed the safety and efficacy of the TSolution One in comparison with traditional knee replacement using manual surgical instrumentation. Study enrollment was completed in December 2018 and included 115 patients.

The surgeons who participated in the study included Bernard Stulberg in Cleveland; Yair David Kissin in Hackensack, N.J.; Stefan Kreuzer in Houston; Ralph Liebelt in Durham, N.C.; and William Long in New York.

“What will be particularly appealing to surgeons is the open implant library offered by this active robotic system, which can achieve an optimal personalized surgical plan for each patient,” said Dr. Stulberg, an orthopedic surgeon and principal investigator in the U.S. clinical study for TSolution One. “This innovative system will revolutionize the treatment of end-stage knee arthritis by coupling an individualized plan with precise bone cutting technology.”

The post TSolution One robot for total knee replacement receives FDA approval appeared first on The Robot Report.


Source: therobotreport

Leave a Reply