Zimmer Biomet Holdings Inc. announced it received FDA 510(k) clearance for the Rosa One Spine System, which is intended for robotically assisted minimally invasive and complex spine surgeries.
According to a company press release, Rosa One Spine combines robotics and navigation to delivers a real-time patient dynamic-tracking capability. It also features 3-D intraoperative planning software to improve the accuracy and predictability of implant and instrument placement.
“Rosa One Spine functions as a dual robotics and navigation technology solution for minimally invasive and complex thoracolumbar spine procedures,” Aure Bruneau, Zimmer Biomet's group president of spine, CMF and thoracic and surgery-assisting technology, said in the release. “We are extremely excited about the addition of Rosa One Spine to our already released Rosa One Brain and Rosa Knee Systems.”