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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
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51 records meeting your search criteria returned- Product Code: KRO Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
AESCULAP AG ENDURO MENISCAL COMPONENT F2 12MM 10/21/2021
ONKOS SURGICAL ELEOS 09/08/2021
AESCULAP AG COLLECT.NO.QAS KNEE IMPLANTS ROTAT.HINGE 05/12/2021
ONKOS SURGICAL ELEOS 04/06/2021
AESCULAP AG AS ENDURO MENISCAL COMPONENT F3 12MM 12/08/2020
ONKOS SURGICAL ELEOS 10/30/2020
AESCULAP AG COLLECT.NO.QAS KNEE IMPL.MISC./UNKNOWN 07/07/2020
AESCULAP AG COLLECT.NO.QAS KNEE IMPL.MISC./UNKNOWN 04/13/2020
AESCULAP AG COLLECT.NO.QAS KNEE IMPL.MISC./UNKNOWN 04/08/2020
AESCULAP AG AS FEMUR EXTENS.STEM 6° D18X157 CEMENTED 01/30/2020
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