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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 Persona Revision SoluTion Femur. The post FDA grants 510(k) clearance to Zimmer’s new revision knee implant component appeared first on Medical Device Network.
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Zimmer Biomet's Persona Revision SoluTion Femur.
The post FDA grants 510(k) clearance to Zimmer’s new revision knee implant component appeared first on Medical Device Network.
