BEUDAMED
    11 results · 58ms · Sources: EU EUDAMED, US FDA

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    S100

    FDA Adverse Event
    Malfunction ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code KWP·April 12, 2017

    RENOVIS

    FDA Adverse Event
    RENOVIS SURGICAL TECHNOLOGIES·Product code JWH·October 26, 2016

    RENOVIS

    FDA Adverse Event
    Injury ·RENOVIS SURGICAL TECHNOLOGIES·Product code OQI·December 12, 2018

    S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM

    FDA Adverse Event
    Injury ·RENOVIS SURGICAL TECHNOLOGIES·Product code OVD·December 12, 2018

    RENOVIS

    FDA Adverse Event
    Malfunction ·RENOVIS SURGICAL TECHNOLOGIES·Product code OVE·December 28, 2018

    S 100 PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·RENOVIS SURGICAL TECHNOLOGIES·Product code MNI·July 20, 2011

    RENOVIS

    FDA Adverse Event
    Malfunction ·RENOVIS SURGICAL TECHNOLOGIES·Product code OVD·February 1, 2019

    S 150 STAND-ALONE ANTERIOR CERVICAL INTERBODY FUSION

    FDA Adverse Event
    Malfunction ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code OVE·March 22, 2017

    TESERA 3-D PRINTED ALIF CAGE

    FDA Adverse Event
    Injury ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code MAX·July 3, 2018

    A200 KNEE SYSTEM

    FDA Adverse Event
    Injury ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016

    A200 KNEE SYSTEM

    FDA Adverse Event
    Injury ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016