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Zimmer Biomet Receives FDA Clearance for Persona® Revision SoluTion™ Femur – Ortho Spine News

Summary by Ortho Spine News | Your Trusted Voice for Medical Device Industry Ortho News
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 leader, today announced U.S. Food and Drug Administration (FDA) 510(k) clearance of Persona® Revision SoluTion Femur, a revision knee implant component offering an alternative for patients with sensitivities to certain metals. The Persona Revision SoluTio
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Ortho Spine News | Your Trusted Voice for Medical Device Industry Ortho NewsOrtho Spine News | Your Trusted Voice for Medical Device Industry Ortho News

Zimmer Biomet Receives FDA Clearance for Persona® Revision SoluTion™ Femur – Ortho Spine News

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 leader, today announced U.S. Food and Drug Administration (FDA) 510(k) clearance of Persona® Revision SoluTion Femur, a revision knee implant component offering an alternative for patients with sensitivities to certain metals. The Persona Revision SoluTio

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Ortho Spine News | Your Trusted Voice for Medical Device Industry Ortho News broke the news in on Friday, March 7, 2025.
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