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Exactech has received FDA 510(k), clearance for polyethylene knee implants

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Exactech has received FDA 510(k), clearance for polyethylene knee implants



Exactech, in a press statement, announced that its Activit E polyethylene knee for total knee surgery has been cleared by the FDA under 510(k).
According to a release, Activit-E, a highly-cross-linked polyethylene material, is intended to be used along with the Truliant knee-replacement system from Exactech.
“After years of research and development in polyethylene, Activit-E represents a breakthrough achievement for Exactech,” Adam Hayden, chief medical officer and senior vice president of the large joints business unit at Exactech, said in the release. “It is the next generation of



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