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	<title>Personalized Christmas Online &#187; cliftonzil82</title>
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		<title>Gynecare mesh lawsuit</title>
		<link>http://www.personalizedchristmas.net/gynecare-mesh-lawsuit_202005.html</link>
		<comments>http://www.personalizedchristmas.net/gynecare-mesh-lawsuit_202005.html#comments</comments>
		<pubDate>Wed, 29 Aug 2012 19:24:18 +0000</pubDate>
		<dc:creator>cliftonzil82</dc:creator>
				<category><![CDATA[Health]]></category>
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		<description><![CDATA[Seeking Approval for Gynecare Mesh Typically, before releasing a new product on the market, a company must apply for a review and approval from the FDA. Many times, they can opt for the so-called &#8220;fast track&#8221; 510(k) approval program, which requires only that the company show the new device to be significantly similar to one [...]]]></description>
			<content:encoded><![CDATA[<p>Seeking Approval for Gynecare Mesh<br />
Typically, before releasing a new product on the market, a company must apply for a review and approval from the FDA. Many times, they can opt for the so-called &#8220;fast track&#8221; 510(k) approval program, which requires only that the company show the new device to be significantly similar to one that&#8217;s already been approved. </p>
<p>J &amp; J indicated that it based its decision not to apply for 510(k) approval for the Prolift vaginal mesh on the FDA&#8217;s guidance document entitled, &#8220;Deciding When to Submit a 510(k) for a Change to an Existing Device.&#8221; Since it&#8217;s up to companies to decide when to apply for approval, J &amp; J decided that the new Gynecare Prolift was so similar to its previous product, the Gynemesh, that a new review was not necessary.</p>
<p>For more information go to </p>
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