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FDA grants 510(k) clearance to Zimmer’s new revision knee implant component
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Zimmer Biomet's new revision knee implant component, Persona Revision SoluTion Femur, to provide an option for individuals ...
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Zimmer Biomet Receives FDA Clearance for Persona® Revision SoluTion™ Femur
Persona Revision SoluTion Femur will be commercially available in the U.S. in Q3 2025. About Zimmer Biomet Zimmer Biomet is a global medical technology leader with a comprehensive portfolio ...
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Zimmer Biomet's Persona Revision SoluTion Femur Receives FDA 510(k) Clearance
(RTTNews) - Zimmer Biomet Holdings, Inc. (ZBH), Friday announced that the company has received the U.S. Food and Drug Administration 510(k) clearance of Persona Revision SoluTion Femur, a revision ...
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Zimmer Biomet Receives FDA Clearance for Persona® Revision SoluTion™ Femur
WARSAW, Ind., March 7, 2025 /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) ...
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Zimmer Biomet Holdings, Inc.: Zimmer Biomet Receives FDA Clearance for Persona Revision SoluTion Femur
A Revision Knee Implant Alternative for Patients with Metal Sensitivities WARSAW, Ind., March 7, 2025 /PRNewswire/ -- Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global medical technology ...