Zimmer Biomet receives FDA 510(k) clearance for ROSA Knee System

Zimmer Biomet announced U.S. FDA 510(k) clearance of the ROSA Knee System for robotically-assisted total knee replacement surgeries. ROSA Knee features 3D pre-operative planning tools and real-time, intraoperative data on soft-tissue and bone anatomy designed to improve bone cut accuracy and range of motion gap analysis to potentially improve flexion and restoration of natural joint movement.
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