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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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90 records meeting your search criteria returned- Product Code: NIO Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ATRIUM MEDICAL CORPORATION ATRIUM ADVANTA V12 COVERED STENT 02/03/2016
MEDTRONIC IRELAND COMPLETE SE ILIAC 12/17/2015
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 12/11/2015
ATRIUM MEDICAL CORPORATION ATRIUM ADVANTA V12 COVERED STENT 12/08/2015
ATRIUM MEDICAL CORPORATION ATRIUM ADVANTA V12 COVERED STENT 09/30/2015
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 09/21/2015
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 09/15/2015
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG E-LUMINEXX VASCULAR STENT 09/03/2015
BOSTON SCIENTIFIC - MAPLE GROVE EPIC¿ 08/27/2015
BOSTON SCIENTIFIC - GALWAY EXPRESS® LD ILIAC / BILIARY 05/05/2015
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