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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
MEDTRONIC NEUROMODULATION IMPLANTABLE NEUROSTIMULATOR 11/03/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 10/31/2023
MEDTRONIC NEUROMODULATION LEAD 10/27/2023
MEDTRONIC NEUROMODULATION IMPLANTABLE NEUROSTIMULATOR 10/27/2023
MEDTRONIC EUROPE SARL SOLETRA 10/25/2023
MEDTRONIC NEUROMODULATION EXTERNAL NEUROSTIMULATOR 10/23/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 10/18/2023
MEDTRONIC NEUROMODULATION EXTERNAL NEUROSTIMULATOR 10/13/2023
MEDTRONIC EUROPE SARL SOLETRA 10/13/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 10/11/2023
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