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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 IRELAND RESOLUTE ONYX RX 02/22/2023
MEDTRONIC IRELAND RESOLUTE ONYX RX 02/14/2023
MEDTRONIC IRELAND ONYX FRONTIER 02/07/2023
MEDTRONIC IRELAND RESOLUTE INTEGRITY RX 01/23/2023
MEDTRONIC IRELAND ONYX FRONTIER 01/19/2023
MEDTRONIC IRELAND RESOLUTE ONYX RX 01/19/2023
MEDTRONIC IRELAND ONYX FRONTIER 01/17/2023
MEDTRONIC IRELAND RESOLUTE ONYX RX 12/22/2022
MEDTRONIC IRELAND RESOLUTE ONYX RX 12/16/2022
MEDTRONIC IRELAND ENDEAVOR RESOLUTE RX 12/07/2022
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