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	<title>SpineJournal.gr &#124; Spine News &#187; Intrepid</title>
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		<title>FDA Classifies Medtronic Voluntary February Recall for Intrepid™ Intervertebral Body Fusion Device as Class II</title>
		<link>http://www.spinejournal.gr/2009/07/fda-classifies-medtronic-voluntary-february-recall-for-intrepid%e2%84%a2-intervertebral-body-fusion-device-as-class-ii/</link>
		<comments>http://www.spinejournal.gr/2009/07/fda-classifies-medtronic-voluntary-february-recall-for-intrepid%e2%84%a2-intervertebral-body-fusion-device-as-class-ii/#comments</comments>
		<pubDate>Fri, 24 Jul 2009 16:58:05 +0000</pubDate>
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				<category><![CDATA[CE & FDA]]></category>
		<category><![CDATA[fda]]></category>
		<category><![CDATA[Intrepid]]></category>
		<category><![CDATA[Medtronic]]></category>
		<category><![CDATA[recall]]></category>

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		<description><![CDATA[MINNEAPOLIS – July 23, 2009 – Medtronic, Inc. (NYSE: MDT) announced today that the U.S. Food and Drug Administration (FDA) has classified its voluntary recall action of the Intrepid™ Intervertebral Body Fusion Device as a Class II recall. Medtronic initiated a voluntary recall of the product on February 6, 2009, and communicated the risk to physicians [...]]]></description>
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