Medical Device Network on MSN17d
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 ...
Hosted on MSN3mon
Zimmer Biomet’s total shoulder replacement system gains FDA 510(k) clearance
Available in a single instrument tray, the system is suitable for ... a component of its total knee implant system. "Zimmer Biomet’s total shoulder replacement system gains FDA 510(k) clearance ...