BEUDAMED
    23 results · 42ms · Sources: EU EUDAMED, US FDA

    MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Integrated Fixation, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Lumbar

    Appliance, Fixation, Spinal Interlaminal

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