BEUDAMED
    4 results · 28ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    SPINEWORKS ANTERIOR LUMBAR DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LEKSELL SURGIPLAN WITH IMAGEMERGE

    FDA 510(k)
    FDA Class 2 ·Neurology

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Neurological Stereotaxic Instrument

    FDA classification
    FDA Class 2 ·Neurological Stereotaxic Instrument