WARSAW, Ind., Sept. 20, 2022 /PRNewswire/ -- Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global medical technology leader, today announced U.S. Food and Drug Administration (FDA) 510(k) ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Zimmer Biomet received FDA clearance for its OsseoFit ...
CLEVELAND-- Throughout the 2017 season, Indians center fielder Bradley Zimmer became well-known for his speed and defense after being called up last May. It CLEVELAND-- Throughout the 2017 season, ...
The FDA approved Zimmer Biomet’s Sidus stem-free shoulder system. 1. The Sidus system is a total shoulder arthroplasty solution for patients with good bone stock that have osteoarthritis, ...
Zimmer Biomet Holdings, Inc. ZBH recently received FDA 510(k) clearance for the Identity Shoulder System for anatomic, reverse and revision shoulder replacement. The Identity Shoulder System is the ...
The ROSA ® Shoulder System Becomes the First-to-Market Robotic Surgical Assistant for Shoulder Arthroplasty and the Fourth ROSA Robotics Application in Five Years WARSAW, Ind., Feb. 22, 2024 ...
Zimmer Biomet Holdings Inc.’s Rosa robotics surgical assistant snapped up its fourth application with the U.S. FDA’s 510(k) clearance for use in shoulder replacement surgery. Over the past five years, ...