New Anatomically Shaped Asymmetric Stemless Design for Total Shoulder Replacement
WARSAW, Ind., Dec. 13, 2024 /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) clearance for the OsseoFit™ Stemless Shoulder System for total shoulder replacement. This innovative implant is designed to match the natural humeral (upper shoulder bone) anatomy1-3 to optimize anatomical fit while maximizing preservation of healthy bone. The OsseoFit Stemless Shoulder System expands the company's expansive total shoulder portfolio and integrates with Identity® Humeral Heads with Versa-Dial® Technology for infinite offset placement as well as the Alliance® Glenoid for a broad range of glenoid options to adapt to a patient's unique anatomy.
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