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		<title>Minutes from Negotiation Meeting on MDUFA III Reauthorization</title>
		<link>http://www.spinejournal.gr/2011/06/minutes-from-negotiation-meeting-on-mdufa-iii-reauthorization/</link>
		<comments>http://www.spinejournal.gr/2011/06/minutes-from-negotiation-meeting-on-mdufa-iii-reauthorization/#comments</comments>
		<pubDate>Wed, 22 Jun 2011 06:54:23 +0000</pubDate>
		<dc:creator>Akillas</dc:creator>
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		<description><![CDATA[April 13, 2011 FDA – Industry MDUFA III Reauthorization Meeting Purpose To discuss potential financial...]]></description>
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		<title>ReGen Sues FDA Seeking Restoration Of Knee-Device Approval</title>
		<link>http://www.spinejournal.gr/2011/06/regen-sues-fda-seeking-restoration-of-knee-device-approval/</link>
		<comments>http://www.spinejournal.gr/2011/06/regen-sues-fda-seeking-restoration-of-knee-device-approval/#comments</comments>
		<pubDate>Wed, 22 Jun 2011 06:41:37 +0000</pubDate>
		<dc:creator>Akillas</dc:creator>
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		<guid isPermaLink="false">http://www.spinejournal.gr/?p=1634</guid>
		<description><![CDATA[ReGen Biologics Inc. (RGBOQ) has sued the U.S. Food and Drug Administration while seeking to...]]></description>
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		<title>GAO renews critique of FDA medical device system</title>
		<link>http://www.spinejournal.gr/2011/04/gao-renews-critique-of-fda-medical-device-system/</link>
		<comments>http://www.spinejournal.gr/2011/04/gao-renews-critique-of-fda-medical-device-system/#comments</comments>
		<pubDate>Tue, 19 Apr 2011 07:36:38 +0000</pubDate>
		<dc:creator>Akillas</dc:creator>
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		<description><![CDATA[WASHINGTON (AP) — Government investigators say the Food and Drug Administration is putting patients at...]]></description>
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		<title>FDA Issues Non-Approvable Letter for Medtronic&#8217;s Amplify</title>
		<link>http://www.spinejournal.gr/2011/03/fda-issues-non-approvable-letter-for-medtronics-amplify/</link>
		<comments>http://www.spinejournal.gr/2011/03/fda-issues-non-approvable-letter-for-medtronics-amplify/#comments</comments>
		<pubDate>Mon, 14 Mar 2011 07:20:29 +0000</pubDate>
		<dc:creator>Akillas</dc:creator>
				<category><![CDATA[CE & FDA]]></category>
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		<description><![CDATA[BY SANDER DUNCAN, MARCH 11, 2011 Medtronic disclosed in its 10-Q on Wednesday that the...]]></description>
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		<title>Orthovita Receives FDA Clearance for Vitoss(TM) Bimodal Bone Graft Substitute</title>
		<link>http://www.spinejournal.gr/2011/02/orthovita-receives-fda-clearance-for-vitosstm-bimodal-bone-graft-substitute/</link>
		<comments>http://www.spinejournal.gr/2011/02/orthovita-receives-fda-clearance-for-vitosstm-bimodal-bone-graft-substitute/#comments</comments>
		<pubDate>Mon, 14 Feb 2011 07:17:15 +0000</pubDate>
		<dc:creator>Akillas</dc:creator>
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		<category><![CDATA[Vitoss Bimodal]]></category>

		<guid isPermaLink="false">http://www.spinejournal.gr/?p=1182</guid>
		<description><![CDATA[MALVERN, Pa.&#8211;(Healthcare Sales &#038; Marketing Network)&#8211; Orthovita, Inc. (NASDAQ:VITA ), an orthobiologics and biosurgery company,...]]></description>
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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>
		<dc:creator>Akillas</dc:creator>
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		<description><![CDATA[New biologic bone graft product demonstrated superior fusion rates compared to current standard of care...]]></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>
		<dc:creator>Akillas</dc:creator>
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		<description><![CDATA[MINNEAPOLIS – July 23, 2009 – Medtronic, Inc. (NYSE: MDT) announced today that the U.S....]]></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>Akillas</dc:creator>
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		<description><![CDATA[Medtronic received long-awaited FDA approval for its Bryan cervical disc on May 12. The device...]]></description>
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