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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
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8 records meeting your search criteria returned- Product Code: NEK Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 08/03/2015
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 08/03/2015
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 07/28/2015
MEDTRONIC SOFAMOR DANEK USA, INC INFUSE BONE GRAFT 07/22/2015
MEDTRONIC INFUSE BONE GRAFT 06/08/2015
MEDTRONIC BMP7 01/26/2015
MEDTRONIC SOFAMOR DANEK INFUSE BONE GRAFT RHBMP-2/ACS 12/22/2014
MEDTRONIC INFUSE BONE GRAFT 12 MG 05/01/2014
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