Zimmer Biomet Receives FDA Approval for its Rosa System
On 20 April 2021, Zimmer Biomet received FDA 510(k) clearance for its Rosa Partial Knee system for robotically-assisted partial knee replacement surgeries. This is the new edition to Zimmer Biomet's Rosa Robotics platform, which comprises the Rosa Knee system for total knee replacement surgery and Rosa One for neurosurgical and spine procedures.
This system is compatible with Zimmer Biomet's Persona Partial Knee. It has 2D and 3D X-Atlas imaging technology with real-time, intraoperative data collection on soft tissue and bone anatomy to increase bone cut accuracy and range of motion gap analysis.
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