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THORNIER mplants___ChirurgicauxMAY 52011 ___Summary of Safety and Effectiveness informationSpecial SJO(k) PremarketNotification HLS KNEE leg System Date prepared: May5t, 2011Regulatory authority:
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wwwaccessdatafdagov cdrhdocs pdf9tornier is a form required by the FDA for medical device manufacturers to report information about their devices.
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