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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
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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86 records meeting your search criteria returned- Product Code: MFR Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MEDTRONIC NEUROMODULATION UNKNOWN IMPLANTABLE NEUROSTIMULATOR 03/13/2018
MEDTRONIC NEUROMODULATION UNKNOWN IMPLANTABLE NEUROSTIMULATOR 02/01/2018
MEDTRONIC NEUROMODULATION UNKNOWN IMPLANTABLE NEUROSTIMULATOR 07/10/2017
MEDTRONIC NEUROMODULATION unknown brand name 06/30/2017
MEDTRONIC NEUROMODULATION unknown brand name 06/08/2017
MEDTRONIC NEUROMODULATION UNKNOWN IMPLANTABLE NEUROSTIMULATOR 06/05/2017
MEDTRONIC NEUROMODULATION unknown brand name 05/31/2017
MEDTRONIC NEUROMODULATION ACTIVA 05/02/2017
MEDTRONIC NEUROMODULATION UNKNOWN IMPLANTABLE NEUROSTIMULATOR 01/31/2017
MEDTRONIC NEUROMODULATION UNKNOWN DEEP BRAIN NEUROSTIMULATOR 12/22/2016
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