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Home » Zimmer Biomet’s Revision Knee System Cleared by FDA
Zimmer Biomet’s Revision Knee System Cleared by FDA
![ClearanceStamp_Blue.gif](https://www.fdanews.com/ext/resources/test/Device_Images6/ClearanceStamp_Blue.gif?t=1576043968&width=430)
November 2, 2018
The FDA granted 510(k) clearance for Zimmer Biomet’s Persona revision knee system for use in revision knee replacement procedures.
The knee system enables surgeons to perform simple and complex revision procedures using their preferred approach.
It is matched according to a patient’s anatomy to achieve a personal fit.
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