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	<title>SpineJournal.gr &#187; fda</title>
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		<title>Medtronic&#8217;s AMPLIFY rhBMP-2 Matrix Receives Positive Votes from FDA</title>
		<link>http://www.spinejournal.gr/2010/07/medtronics-amplify-rhbmp-2-matrix-receives-positive-votes-from-fda/</link>
		<comments>http://www.spinejournal.gr/2010/07/medtronics-amplify-rhbmp-2-matrix-receives-positive-votes-from-fda/#comments</comments>
		<pubDate>Wed, 28 Jul 2010 06:51:18 +0000</pubDate>
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				<category><![CDATA[CE & FDA]]></category>
		<category><![CDATA[News]]></category>
		<category><![CDATA[amplify]]></category>
		<category><![CDATA[bone graft]]></category>
		<category><![CDATA[fda]]></category>
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		<category><![CDATA[Medtronic]]></category>

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		<description><![CDATA[New biologic bone graft product demonstrated superior fusion rates compared to current standard of care for complex fusion procedures of the lower spine in the pivotal clinical trial.
MINNEAPOLIS&#8211;(HSMN NewsFeed)&#8211;The U.S. Food and Drug Administration (FDA) Orthopaedic and Rehabilitation Devices Panel today voted 9 for and 4 against (1 abstention) on safety and 10 for and [...]]]></description>
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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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		<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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		<title>FDA Approves Medtronic&#8217;s Bryan Cervical Disc</title>
		<link>http://www.spinejournal.gr/2009/05/fda-approves-medtronics-bryan-cervical-disc/</link>
		<comments>http://www.spinejournal.gr/2009/05/fda-approves-medtronics-bryan-cervical-disc/#comments</comments>
		<pubDate>Sat, 30 May 2009 07:50:58 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[CE & FDA]]></category>
		<category><![CDATA[Products Launch]]></category>
		<category><![CDATA[Bryan]]></category>
		<category><![CDATA[cervical disc]]></category>
		<category><![CDATA[fda]]></category>
		<category><![CDATA[Medtronic]]></category>

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		<description><![CDATA[Medtronic received long-awaited FDA approval for its Bryan cervical disc on May 12.  The device received a favorable FDA panel recommendation in July of 2007, just a day after Medtronic&#8217;s Prestige disc was approved for market launch. Under the conditions for Bryan&#8217;s approval, Medtronic will conduct a 10-year post-market study tracking patients&#8217; neck disability [...]]]></description>
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