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	<title><![CDATA[fda and ide Resources | BNET]]></title>
	<link><![CDATA[http://resources.bnet.com/topic/fda+and+ide.html]]></link>
	<description><![CDATA[White papers, case studies, business articles, and blog posts relating to fda and ide]]></description>
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		<title><![CDATA[Spinal Restoration, Inc. Receives FDA IDE Approval]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2008_May_13/ai_n25408357]]></link>
		<description><![CDATA[AUSTIN, Texas -- Spinal Restoration, Inc. announced today that the U.S. Food and Drug Administration has approved an Investigational Device Exemption IDE pilot study of the Biostat([R])Disc Augmentation System. Enrollment in the 15 patient pilot study is expected to begin at three clinical sites in July.]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Tue, 13 May 2008 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
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	<item>
		<title><![CDATA[Imaging3 Receives FDA Approval to Distribute the Dominion Vi Scanner Under FDA (IDE) Regulations]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_pwwi/is_200804/ai_n24972432]]></link>
		<description><![CDATA[Imaging3TM, Inc. (OTCBB: IMGG), developer of a breakthrough medical imaging device that produces 3D medical diagnostic images of virtually any part of the human body in real-time, today provided insight into the Company's progress with the FDA.  "This is a very important step in the FDA 510k approval process...]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Wed, 02 Apr 2008 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
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	<item>
		<title><![CDATA[Cook Incorporated Files IDE Application for Zenith Branch Vessel Graft with U.S. FDA]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2008_Jan_24/ai_n24221520]]></link>
		<description><![CDATA[BLOOMINGTON, Ind. -- Cook Incorporated, the world leader in endovascular repair of aortic disease, has filed an Investigational Device Exemption IDE for a new type of endograft designed to treat patients with aortoiliac or iliac aneurysms that have been difficult to treat endovascularly with currently available designs.]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Thu, 24 Jan 2008 00:00:00 -0800</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
	</item>
	<item>
		<title><![CDATA[ViaCell Receives IDE Supplement Approval to Advance ViaCyte Pivotal Trial]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2007_July_9/ai_n19345663]]></link>
		<description><![CDATA[CAMBRIDGE, Mass. -- ViaCell, Inc. (Nasdaq: VIAC) announced today that it has received FDA approval of its investigational device exemption IDE supplement for its ViaCyteSM pivotal clinical trial. The pivotal study will evaluate ViaCyte, an investigational product being studied for the cryopreservation and thawing of human oocytes for use during...]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Mon, 09 Jul 2007 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
	</item>
	<item>
		<title><![CDATA[FDA Grants IDE Approval to TransMedics for the Pilot Phase of the PROCEED Clinical Trial for Its Organ Care System&#153; - the First System to Support Beating Heart Transplant]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2007_April_19/ai_n27207552]]></link>
		<description><![CDATA[ANDOVER, Mass. -- TransMedics, Inc., an emerging medical technology company developing advanced solutions for better, more organ transplant technologies, announced today it has received IDE approval to initiate the pilot phase of the PROCEED multi-center clinical trial in the U.S. for its Organ Care System[TM]. The PROCEED trial will evaluate...]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Thu, 19 Apr 2007 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/clinical+trial.html"><![CDATA[clinical trial]]></category>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
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	<item>
		<title><![CDATA[CVRx®, Inc., Receives IDE Approval for Rheos&#153; Baroreflex Hypertension Therapy&#153; System Pivotal Trial]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2006_Oct_16/ai_n27038305]]></link>
		<description><![CDATA[MINNEAPOLIS -- CVRx([R]), Inc., a private medical device company that has developed an implantable medical device to treat high blood pressure, has received a conditional investigational device exemption IDE approval from the U.S. Food and Drug Administration FDA to begin a U.S. pivotal clinical trial that will evaluate the safety...]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Mon, 16 Oct 2006 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
	</item>
	<item>
		<title><![CDATA[FDA Approves Abiomed's IDE for IMPELLA 5.0 Minimally Invasive Cardiac Support Systems; Advanced Medical Technology Indicated for Use with Low Cardiac Output after Cardiac Surgery]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2006_June_27/ai_n26907964]]></link>
		<description><![CDATA[DANVERS, Mass. -- Abiomed, Inc. (NASDAQ: ABMD) today announced conditional approval by the U.S. Food and Drug Administration FDA of its Investigational Device Exemption IDE for the IMPELLA 5.0 unique, catheter-based Circulatory Support Systems. Clinical trials in the U.S. are to begin immediately. The IMPELLAR RECOVER 5.0 devices are already...]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Tue, 27 Jun 2006 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
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	<item>
		<title><![CDATA[FDA Approves 'IDE' Clinical Trial of Paradigm Spine's Coflex(TM) Functionally Dynamic Interspinous Implant.]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_hb5570/is_200605/ai_n23538193]]></link>
		<description><![CDATA[NEW YORK, May 9 /PRNewswire/ --    NEW YORK, May 9 /PRNewswire/ --  ]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Tue, 09 May 2006 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/clinical+trial.html"><![CDATA[clinical trial]]></category>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
	</item>
	<item>
		<title><![CDATA[FDA Approves Further Changes To CORTOSS® IDE Pivotal Study Protocol]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2006_April_17/ai_n16125685]]></link>
		<description><![CDATA[MALVERN, Pa. -- Orthovita, Inc.]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Mon, 17 Apr 2006 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/pivotal+corp..html"><![CDATA[Pivotal Corp.]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
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	<item>
		<title><![CDATA[Outpatient Procedure for Asthma; Asthmatx Announces the Start of its FDA Approved IDE Study that may Change the Course of Asthma Care]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2006_Jan_9/ai_n15990283]]></link>
		<description><![CDATA[MOUNTAIN VIEW, Calif. -- Asthmatx, Inc. today announced the start of its Asthma Intervention Research 2 (AIR2) Trial of its catheter-based investigational procedure that may change the standard of care for millions of asthma sufferers.]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Mon, 09 Jan 2006 00:00:00 -0800</pubDate>
		<category domain="http://resources.bnet.com/topic/asthma.html"><![CDATA[asthma]]></category>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
	</item>
	<item>
		<title><![CDATA[Angiotech Pharmaceuticals: Boston Scientific Submits Amended IDE to FDA for U.S. Clinical Trial of its Paclitaxel-Eluting Coronary Stent System.]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_hb5559/is_200202/ai_n22626282]]></link>
		<description><![CDATA[VANCOUVER, BRITISH COLUMBIA, FEBRUARY 20, 2002    VANCOUVER, BRITISH COLUMBIA, FEBRUARY 20, 2002  ]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Wed, 20 Feb 2002 00:00:00 -0800</pubDate>
		<category domain="http://resources.bnet.com/topic/boston+scientific+corp..html"><![CDATA[Boston Scientific Corp.]]></category>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
		<category domain="http://rss.financialcontent.com/stocksymbol">BSX</category>
		<category domain="tickers">BSX</category>
	</item>
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		<title><![CDATA[Angiotech Pharmaceuticals: Boston Scientific Submits Amended IDE to FDA for U.S. Clinical Trial of Its Paclitaxel-Eluting Coronary Stent System]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2002_Feb_20/ai_83089537]]></link>
		<description><![CDATA[Business Editors & Health/Medical Writers]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Wed, 20 Feb 2002 00:00:00 -0800</pubDate>
		<category domain="http://resources.bnet.com/topic/boston+scientific+corp..html"><![CDATA[Boston Scientific Corp.]]></category>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
		<category domain="http://rss.financialcontent.com/stocksymbol">BSX</category>
		<category domain="tickers">BSX</category>
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		<title><![CDATA[Angiotech Pharmaceuticals: Boston Scientific Submits IDE to FDA for U.S. Clinical Trial of its Paclitaxel-Eluting Coronary Stent System; Trial is Company's Fourth.]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_hb5559/is_200110/ai_n22619278]]></link>
		<description><![CDATA[NATICK, MASSACHUSETTS, OCTOBER 25, 2001    NATICK, MASSACHUSETTS, OCTOBER 25, 2001  ]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Thu, 25 Oct 2001 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/boston+scientific+corp..html"><![CDATA[Boston Scientific Corp.]]></category>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
		<category domain="http://rss.financialcontent.com/stocksymbol">BSX</category>
		<category domain="tickers">BSX</category>
	</item>
	<item>
		<title><![CDATA[Angiotech Pharmaceuticals: Boston Scientific Submits IDE to FDA for U.S. Clinical Trial of its Paclitaxel-Eluting Coronary Stent System]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2001_Oct_25/ai_79444971]]></link>
		<description><![CDATA[Business Editors]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Thu, 25 Oct 2001 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/boston+scientific+corp..html"><![CDATA[Boston Scientific Corp.]]></category>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
		<category domain="http://rss.financialcontent.com/stocksymbol">BSX</category>
		<category domain="tickers">BSX</category>
	</item>
	<item>
		<title><![CDATA[EndoSonics Submits IDE Application to the FDA for Directional Brachytherapy Device; Cleveland Clinic Foundation is Development Partner]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_2000_March_28/ai_60828554]]></link>
		<description><![CDATA[Business Editors and Medical/Health Writers]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Tue, 28 Mar 2000 00:00:00 -0800</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
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	<item>
		<title><![CDATA[Thoratec Files IDE for Vascular Access Graft; Data Allows FDA to Determine Whether Clinical Trials Can Commence]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_1997_Dec_4/ai_20033903]]></link>
		<description><![CDATA[PLEASANTON, Calif.--BW HealthWire--Dec. 4, 1997--Thoratec Laboratories Corporation (NASDAQ:THOR), a medical device company, today announced that it has filed an investigational device exemption IDE for its vascular access graft VAG.]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Thu, 04 Dec 1997 00:00:00 -0800</pubDate>
		<category domain="http://resources.bnet.com/topic/clinical+trial.html"><![CDATA[clinical trial]]></category>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
	</item>
	<item>
		<title><![CDATA[EP MedSystems Files Alert System IDE With FDA]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_1997_August_21/ai_19683527]]></link>
		<description><![CDATA[BUDD LAKE, N.J.--BUSINESS WIRE--Aug. 21, 1997--]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Thu, 21 Aug 1997 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
	</item>
	<item>
		<title><![CDATA[Cardima, Inc. Receives FDA Approval of IDE for Initial Phase of Atrial Fibrillation Study]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_1997_July_9/ai_19576511]]></link>
		<description><![CDATA[FREMONT, Calif.--BW HealthWire--July 9, 1997--Cardima, Inc., (NASDAQ:CRDM) announced today that the FDA had approved the Company's investigational device exemption IDE submission to begin its initial atrial fibrillation AF study in the United States for the Cardima Pathfinder microcatheter system.]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Wed, 09 Jul 1997 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
	</item>
	<item>
		<title><![CDATA[Influence announces Investigational Device Exemption - IDE - and grant of expedited review for the In-Flow incontinence product by FDA]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_1997_May_21/ai_19426420]]></link>
		<description><![CDATA[SAN FRANCISCO--BW HealthWire--May 21, 1997--Influence Inc. announced that the U.S. Food and Drug Administration FDA has granted Investigational Device Exemption IDE for the company's In-FlowTM remote-controlled intraurethral valve-pump catheter.]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Wed, 21 May 1997 00:00:00 -0700</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
	</item>
	<item>
		<title><![CDATA[Life Medical Sciences initiates U.S. clinical trials for REPEL; investigational device exemption  application approved by FDA - IDE]]></title>
		<link><![CDATA[http://findarticles.com/p/articles/mi_m0EIN/is_1997_Feb_18/ai_19133112]]></link>
		<description><![CDATA[EDISON, N.J.--BW HealthWire--Feb. 18, 1997--Life Medical Sciences Inc.(NASDAQ NM:CHAI) Tuesday announced the initiation of US clinical trials of REPEL, the company's bioresorbable barrier film for the prevention/reduction of post-operative adhesions.]]></description>
		<s:doctype><![CDATA[Research articles]]></s:doctype>
		<pubDate>Tue, 18 Feb 1997 00:00:00 -0800</pubDate>
		<category domain="http://resources.bnet.com/topic/fda.html"><![CDATA[FDA]]></category>
		<category domain="http://resources.bnet.com/topic/ide.html"><![CDATA[IDE]]></category>
		<category domain="http://resources.bnet.com/topic/.html"><![CDATA[]]></category>
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