The goal of this prospective, non‐randomized, multicenter clinical trial is to determine
whether robotic‐assisted total knee arthroplasty performed with TSolution One® System is safe
and effective for use as an alternative to the conventional manual techniques. Clinical and
radiographic outcomes for robotic‐assisted total knee arthroplasty performed with the
TSolution One® System will be collected preoperatively, intraoperatively, and postoperatively
up to a follow‐up period of no less than 6 months and no more than 12 months. These outcomes
will be compared to the ones reported in the literature for conventional manual techniques.