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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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147 records meeting your search criteria returned- Product Code: LNQ Product Problem: Break Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ENTERRA 05/16/2016
MEDTRONIC NEUROMODULATION ENTERRA 02/18/2016
MEDTRONIC NEUROMODULATION ENTERRA 02/18/2016
MEDTRONIC NEUROMODULATION ENTERRA 12/28/2015
MEDTRONIC NEUROMODULATION ENTERRA 12/28/2015
MEDTRONIC NEUROMODULATION ENTERRA 12/23/2015
MEDTRONIC NEUROMODULATION ENTERRA 12/04/2015
MEDTRONIC NEUROMODULATION ENTERRA 12/04/2015
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ENTERRA 10/21/2015
MDT SOFAMOR DANEK PUERTO RICO MFG ENTERRA 10/02/2015
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