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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 PUERTO RICO OPERATIONS CO. INTERSTIM 08/10/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. INTERSTIM II 07/28/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. INTERSTIM 07/27/2022
MEDTRONIC NEUROMODULATION INTERSTIM II 07/27/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. INTERSTIM X 06/29/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. INTERSTIM II 06/28/2022
MEDTRONIC NEUROMODULATION INTERSTIM II 06/24/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. INTERSTIM X 06/21/2022
MEDTRONIC NEUROMODULATION INTERSTIM II 06/14/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. INTERSTIM X 05/27/2022
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