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Zimmer Biomet receives FDA clearance for ROSA Shoulder System
The Fly

Zimmer Biomet receives FDA clearance for ROSA Shoulder System

Zimmer Biomet announced U.S. FDA 510(k) clearance of the ROSA Shoulder System for robotic-assisted shoulder replacement surgery. ROSA Shoulder is the world’s first robotic surgery system for shoulder replacement, and the fourth application for the company’s comprehensive ROSA Robotics portfolio, which includes the ROSA Knee System for total knee arthroplasty and ROSA Hip System for total hip replacement. ROSA Shoulder will be commercially available in the U.S. in the second half of 2024, and will work with the mymobility Digital Care Management Platform to bolster the ZBEdge Dynamic Intelligence portfolio for patients undergoing shoulder replacement surgery.

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