BEUDAMED
    6 results · 30ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    Renovis S141 Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMBI 8 MAX

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Appliance, Fixation, Spinal Interlaminal

    FDA classification
    FDA Class 2 ·Appliance, Fixation, Spinal Interlaminal

    Stimulator, Muscle, Powered

    FDA classification
    FDA Class 2 ·Stimulator, Muscle, Powered