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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.
Medical device manufacturers are required to file wwwaccessdatafdagov cdrhdocs pdf9tornier.
wwwaccessdatafdagov cdrhdocs pdf9tornier can be filled out online on the FDA's website or submitted via mail.
The purpose of wwwaccessdatafdagov cdrhdocs pdf9tornier is to ensure that medical devices are safe and effective for use.
Information such as device classification, intended use, labeling, and adverse events must be reported on wwwaccessdatafdagov cdrhdocs pdf9tornier.
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