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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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83 records meeting your search criteria returned- Product Code: LWR Product Problem: Occlusion Within Device Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
MEDTRONIC HEART VALVE DIVISION FREESTYLE AORTIC ROOT BIOPROSTHESIS 12/14/2017
MEDTRONIC HEART VALVE DIVISION FREESTYLE AORTIC ROOT BIOPROSTHESIS 12/07/2017
MEDTRONIC HEART VALVE DIVISION HANCOCK 11/30/2017
MEDTRONIC HEART VALVE DIVISION VALVE HANCOCK II AORTIC CINCH 25 11/30/2017
MEDTRONIC HEART VALVE DIVISION HANCOCK AORTIC BIOPROSTHETIC HEART VALV 11/27/2017
MEDTRONIC HEART VALVE DIVISION MOSAIC 11/20/2017
MEDTRONIC HEART VALVE DIVISION MOSAIC MITRAL BIOPROSTHETIC HEART VALVE 11/20/2017
MEDTRONIC HEART VALVE DIVISION MOSAIC 11/16/2017
MEDTRONIC HEART VALVE DIVISION FREESTYLE AORTIC ROOT BIOPROSTHESIS 11/14/2017
MEDTRONIC HEART VALVE DIVISION MOSAIC AORTIC BIOPROSTHETIC HEART VALVE 11/10/2017
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