BEUDAMED
    4 results · 22ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    PATHWAY ELECTROMYOGRAPH

    FDA 510(k)
    FDA Class 2 ·Neurology

    Device, Biofeedback

    FDA classification
    FDA Class 2 ·Device, Biofeedback

    CONCORDE LIFT™

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Bone Graft, Lumbar

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