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FDA Determines Knee Device Should Not Have Been Cleared for Marketing

The U.S. Food and Drug Administration today announced that an orthopedic device used in the knee should not have been cleared for marketing in the United States. The announcement follows a re-evaluation of the scientific evidence that was undertaken after a September 2009 agency report...

U.S. Food & Drug Administration
Oct 14, 2010

FDA Determines Knee Device Should Not Have Been Cleared for Marketing

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