BEUDAMED
    46 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code MJO·December 20, 2017

    CHAMELEON FACETFUSE MIS SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC.·Product code MRW·June 17, 2010

    PEDFUSE KRD1 PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code MNI·June 8, 2010

    PEDFUSE

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC·Product code MNI·October 17, 2017

    PEDFUSE

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC·Product code MNH·October 13, 2017

    VEGA SPAN SPINOUS PROCESS PLATE SYSTEM

    FDA Adverse Event
    Injury ·SPINEFRONTIER INC.·Product code KWP·October 9, 2017

    INDUS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC·Product code KWQ·October 9, 2017

    INDUS INVUE TIPPED DRIVER

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code HAW·May 21, 2012

    RESPOND REDUCTION SCREW

    FDA Adverse Event
    Other ·SPINEFRONTIER, INC.·Product code MRW·May 31, 2012

    PEDFUSE

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC·Product code MNH·October 17, 2017

    PEDFUSE

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC·Product code MNH·October 12, 2017

    FACETFUSE SCREWS

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC.·Product code MRW·March 20, 2013

    PEDFUSE CROSS CONNECTOR DRIVER

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC.·Product code LXH·March 12, 2013

    FACETFUSE DRIVER

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC.·Product code LXH·March 12, 2013

    PEDFUSE RESET PEDICLE SCREW

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC.·Product code MNI·February 24, 2014

    PEDFUSE PEDICLE SCREW

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC.·Product code MNI·February 24, 2014

    DORADO INTERVERTEBRAL BODY CAGE

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code MAX·April 23, 2009

    CHAMELEON FACETFUSE MIS SCREW SYSTEM

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code MRW·December 17, 2010

    T-HANDLE WITH STRIKE PLATE

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC.·Product code LXH·September 29, 2011

    PEDFUSE

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC.·Product code MNI·September 11, 2014