BEUDAMED
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    Filters FDA Adverse Event ×

    UNKNOWN DEPUY AMK CR TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·June 16, 2014

    COBALT G HV BONE CEMENT

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code LOD·October 19, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 13, 2012