BEUDAMED
    721 results · 57ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VAULT STAND ALONE ALIF SYSTEM

    FDA Adverse Event
    Malfunction ·Product code MAX·October 3, 2012

    SPINALUSA

    FDA Adverse Event
    Malfunction ·SPINAL USA·Product code KWQ·October 20, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 24, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 19, 2017

    SPINAL USA

    FDA Adverse Event
    Malfunction ·SPINAL USA·Product code HXX·October 20, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 26, 2013

    SPINAL USA TRAY / SPINAL S-LOK SCREW

    FDA Adverse Event
    Injury ·PRECISION SPINE, INC.·Product code MNI·December 26, 2019

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 12, 2013

    SPINAL USA SACRAL SCREWS

    FDA Adverse Event
    Injury ·SPINAL USA·Product code KWP·February 15, 2016

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·June 9, 2017

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 24, 2015

    SLIMPLICITY

    FDA Adverse Event
    Injury ·SPINAL USA·Product code KWQ·May 16, 2012

    SLC 6550 POLYAXIAL SCREWS

    FDA Adverse Event
    Malfunction ·SPINAL USA·Product code MNI·May 3, 2011

    NONE

    FDA Adverse Event
    Malfunction ·SPINAL USA·Product code KWQ·August 14, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 20, 2014

    REFORM POLYAXIAL DRIVER

    FDA Adverse Event
    Malfunction ·SPINAL USA, INC·Product code LXH·September 23, 2013

    EASYSPINE SCREW, UNKOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code NKB·August 17, 2020

    S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code MNI·July 30, 2013

    S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code MNI·July 30, 2013

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    FDA Adverse Event
    Malfunction ·SPINAL USA LLC·Product code KWP·September 28, 2011