BEUDAMED
    27 results · 119ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SUMMIT 5.25 OCCIPITAL BONE SCREW, 8MM

    FDA Adverse Event
    Injury ·DEPUY SPINE, INC.·Product code HWC·June 15, 2006

    SUMMIT SYSTEM

    FDA Adverse Event
    Other ·DEPUY ACROMED, INC.·Product code HWC·September 1, 2000

    SUMMIT SET SCREW.

    FDA Adverse Event
    Injury ·DEPUY RAYNHAM·Product code KWP·December 5, 2012

    UNK - SCREW/ROD CONSTRUCT ACCESSORIES: SUMMIT

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL CH·Product code HWC·May 23, 2022

    UNK - PLATES: SUMMIT SI OCT

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL CH·Product code HRS·May 23, 2022

    SUMMIT 5.25 OCCIPITAL BONE SCREW, 8MM

    FDA Adverse Event
    Injury ·DEPUY SPINE, INC.·Product code HWC·June 15, 2006

    SUMMIT 5.25 OCCIPITAL BONE SCREW, 8MM

    FDA Adverse Event
    Injury ·DEPUY SPINE, INC.·Product code HWC·June 15, 2006

    SUMMIT 5.25 OCCIPITAL BONE SCREW, 11MM

    FDA Adverse Event
    Injury ·DEPUY SPINE, INC.·Product code HWC·June 15, 2006

    SUMMIT 5.25 OCCIPITAL BONE, SCREW, 8MM

    FDA Adverse Event
    Injury ·DEPUY SPINE, INC.·Product code HWC·June 15, 2006

    SUMMIT SCREW

    FDA Adverse Event
    Injury ·DEPUY SYNTHES SPINE·Product code KWQ·December 22, 2014

    SUMMIT SCREW

    FDA Adverse Event
    Injury ·DEPUY SYNTHES SPINE·Product code KWQ·December 22, 2014

    OCPTL INV-Y PLATE ASSY, 37MM

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code KWP·April 3, 2018

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SAFAMER DANEK USA, INC.·Product code NEK·January 16, 2007

    MOUNTAINEER OCT MINIPOLYAXIAL SCREWDRIVER

    FDA Adverse Event
    Malfunction ·DEPUY RAYNHAM·Product code LXH·July 27, 2012

    UNK - PLATES: SPINE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code MNH·May 5, 2022

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 22, 2015

    TRIAL CORAIL REVISION STEM 13

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·June 23, 2014

    CORAIL BROACH HANDLE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·June 23, 2014

    COLLECT.NO.QAS SPINE CERVICAL STABILIS.

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code KWQ·March 11, 2020

    UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code ODP·June 30, 2021