<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>
<channel>
	<title>Surgical Product Guide &#187; Medtronic</title>
	<atom:link href="http://blog.surgicalproductguide.com/tag/medtronic/feed/" rel="self" type="application/rss+xml" />
	<link>http://blog.surgicalproductguide.com</link>
	<description>A comprehensive guide to surgical products for medical professionals </description>
	<lastBuildDate>Wed, 05 Jan 2011 20:37:46 +0000</lastBuildDate>
	<language>en</language>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
	<generator>http://wordpress.org/?v=3.1.3</generator>
		<item>
		<title>FDA Concerned with Cancer Rates for New Spine Device</title>
		<link>http://blog.surgicalproductguide.com/2010/07/27/fda-concerned-with-cancer-rates-for-new-spine-device/</link>
		<comments>http://blog.surgicalproductguide.com/2010/07/27/fda-concerned-with-cancer-rates-for-new-spine-device/#comments</comments>
		<pubDate>Tue, 27 Jul 2010 08:39:07 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Surgical Instruments]]></category>
		<category><![CDATA[Amplify device]]></category>
		<category><![CDATA[cancer]]></category>
		<category><![CDATA[degenerative disc disease]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[Medtronic]]></category>
		<category><![CDATA[morphogenetic protein]]></category>
		<category><![CDATA[spinal fusion]]></category>
		<category><![CDATA[spine device]]></category>
		<category><![CDATA[vertebrae rhBMP-2]]></category>
		<guid isPermaLink="false">http://www.surgicalproductguide.com/blog/?p=256</guid>
		<description><![CDATA[FDA reviewers expressed concern with the increased number of cancer cases seen in degenerative disc disease patients implanted with an investigational Medtronic spine device compared with patients who underwent spinal fusion. The Amplify device stabilizes lower back vertebrae in patients with degenerative disc disease by using a compression resistant matrix and a metallic posterior spinal [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://blog.surgicalproductguide.com/files/2010/07/Food-and-Drug-Administration.png"><img class="alignleft size-full wp-image-257" style="margin: 5px" src="http://blog.surgicalproductguide.com/files/2010/07/Food-and-Drug-Administration.png" border="0" alt="Food and Drug Administration" width="200" height="46" /></a>FDA reviewers expressed concern with the increased number of cancer cases seen in degenerative disc disease patients implanted with an investigational Medtronic spine device compared with patients who underwent spinal fusion. The Amplify device stabilizes lower back vertebrae in patients with degenerative disc disease by using a compression resistant matrix and a metallic posterior spinal instrument. Amplify contains rhBMP-2, a morphogenetic protein that is added to the device to spur the formation of new bone.</p>
<p>Read the full story <a href="http://www.medpagetoday.com/ProductAlert/DevicesandVaccines/21393" target="_blank">here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.surgicalproductguide.com/2010/07/27/fda-concerned-with-cancer-rates-for-new-spine-device/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>FDA Okays Bryan Cervical Disc</title>
		<link>http://blog.surgicalproductguide.com/2009/07/03/fda-okays-bryan-cervical-disc/</link>
		<comments>http://blog.surgicalproductguide.com/2009/07/03/fda-okays-bryan-cervical-disc/#comments</comments>
		<pubDate>Fri, 03 Jul 2009 05:03:04 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[FDA Approval]]></category>
		<category><![CDATA[Surgical Instruments]]></category>
		<category><![CDATA[BRYAN]]></category>
		<category><![CDATA[Bryan Cervical Disc]]></category>
		<category><![CDATA[cervical disc]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[Food and Drug Administration]]></category>
		<category><![CDATA[Medtronic]]></category>
		<category><![CDATA[myelopathy]]></category>
		<category><![CDATA[radiculopathy]]></category>
		<guid isPermaLink="false">http://www.surgicalproductguide.com/blog/2009/07/03/fda-okays-bryan-cervical-disc/</guid>
		<description><![CDATA[The US Food and Drug Administration (FDA) has approved a novel artificial cervical disc, BRYAN, for the treatment of single-level cervical disc diseases like radiculopathy and/or myelopathy. The titanium-polyurethane disc, developed by Medtronic Inc, is implanted in milled pockets of adjacent vertebral bodies from C3-C7 to substitute a diseased or bulging natural cervical disc.]]></description>
			<content:encoded><![CDATA[<p><img src="http://blog.surgicalproductguide.com/files/2009/07/medtronic.png" align="left" vspace="5" width="200" height="47" hspace="5" />The US Food and Drug Administration (FDA) has approved a novel artificial cervical disc, BRYAN, for the treatment of single-level cervical disc diseases like radiculopathy and/or myelopathy. The titanium-polyurethane disc, developed by Medtronic Inc, is implanted in milled pockets of adjacent vertebral bodies from C3-C7 to substitute a diseased or bulging natural cervical disc.</p>
]]></content:encoded>
			<wfw:commentRss>http://blog.surgicalproductguide.com/2009/07/03/fda-okays-bryan-cervical-disc/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
	</channel>
</rss>

