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Approval follows multi-center investigational clinical trial evaluating the safety and efficacy of TSolution One Total Knee Application.
October 10, 2019
By: PR Newswire
THINK Surgical Inc. has obtained clearance from the U.S. Food and Drug Administration (FDA) to market the TSolution One Total Knee Application for use in total knee arthroplasty (TKA) in the United States. TSolution One is a fully active robot which was previously awarded CE marking and has been actively marketed in Asia Pacific and European markets. More than 550 TKA procedures have been successfully completed worldwide with the TSolution One Total Knee Application to date. “We are thrilled to expand the use of this state-of-the-art technology, which is truly transforming orthopedic surgery,” said John Hahn, CEO and president of THINK Surgical Inc. “U.S. 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. This significant achievement is a testament to our team’s dedication, and I am grateful for their hard work in making this vision a reality.” The TSolution One Total Knee Application includes CT-based 3D pre-surgical planning software which allows the surgeon to design and prepare, in a virtual environment, the patient’s unique knee joint replacement plan using a choice of knee implant options. During total knee replacement surgery, the surgeon implements the patient’s pre-planned procedure using the robot, which prepares the joint according to the surgeon’s plan for precise placement of knee implants. Five surgeons participated in the clinical trial, which confirmed the safety and efficacy of the TSolution One Total Knee Application compared to traditional knee replacement using manual surgical instrumentation. Study enrollment was completed in December 2018 and included 115 patients. The following surgeons participated in the study:
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