BEUDAMED
    14 results · 40ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    PROSTHESIS, INTERVERTEBRAL DISC

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

    PEDFUSE KRD1 PEDICLE SCREW SYSTEM

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

    VEGA SPAN SPINOUS PROCESS PLATE SYSTEM

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

    INDUS INVUE TIPPED DRIVER

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

    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

    DORADO INTERVERTEBRAL BODY CAGE

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code MAX·July 21, 2009

    DORADO INTERVERTEBRAL BODY CAGE

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code MAX·July 21, 2009

    S-LIF INTERVERTEBRAL BODY FUSION DEVICE

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code MAX·June 17, 2011

    THREADED GUIDEWIRE 1.6MM X 500MM

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code LXH·September 8, 2008

    THREADED GUIDEWIRE 1.6MM X 500MM

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code HXI·August 18, 2008

    THREADED GUIDEWIRE 1.6MM X 500MM

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code HXI·August 22, 2008

    THREADED GUIDEWIRE 1.6MM X 500MM

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC.·Product code LXH·September 9, 2008

    PEDFUSE

    FDA Adverse Event
    Injury ·SPINEFRONTIER, INC·Product code MNH·May 2, 2018