If your OR wish list includes fewer debates about alignment philosophy and more time spent actually replacing knees, the FDA just checked a big box for you.
The U.S. Food and Drug Administration has granted 510(k) clearance to an enhanced version of Zimmer Biomet’s ROSA® Knee robotic system — now upgraded with automated kinematic alignment and a suite of surgeon-driven personalization tools branded OptimiZe™. In plain English: the robot doesn’t just execute plans anymore — it adapts to how you think about knees.
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