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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience(MAUDE)
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8 records meeting your search criteria returned- Product Code: MJO Patient Problem: Inadequate Osseointegration Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
LDR MÉDICAL MOBI-C IMPLANT "M" STANDARD, UNKNOWN SIZ 09/21/2021
LDR MÉDICAL MOBI-C IMPLANT "M" STANDARD, UNKNOWN SIZ 09/21/2021
AESCULAP AG COLLECT.NO.QAS SPINE INTERBODY FUSION 10/01/2020
AESCULAP AG ACTIV L PE-INLAY 8.5MM 08/07/2020
AESCULAP AG ACTIV L INF.PLATE S1 SIZE M 5/SPIKES 08/07/2020
LDR MÉDICAL MOBI-C IMPLANT, UNKNOWN SIZE 06/25/2019
SYNTHES HAGENDORF PRODISC CERVICAL LARGE/5MM-STERILE 12/10/2015
NUVASIVE, INC. PCM CERVICAL DISC SYSTEM 01/03/2014
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