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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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109 records meeting your search criteria returned- Product Code: NIO Patient Problem: Reocclusion Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC - GALWAY EXPRESS LD ILIAC/BILIARY PREMOUNTED STEN 04/01/2015
BOSTON SCIENTIFIC - GALWAY EXPRESS LD ILIAC/BILIARY PREMOUNTED STEN 03/24/2015
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 02/13/2015
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 01/21/2015
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 01/19/2015
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 12/29/2014
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 12/29/2014
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 12/10/2014
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 12/09/2014
CORDIS CORPORATION SMART CONTROL NITINOL STENT SYSTEM 11/20/2014
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