BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    NuVasive® Modulus XLIF Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE

    FDA 510(k)
    FDA Class 2 ·Neurology

    VIZION DR

    FDA 510(k)
    FDA Class 2 ·Radiology

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    System, X-Ray, Stationary

    FDA classification
    FDA Class 2 ·System, X-Ray, Stationary

    Stimulator, Nerve, Transcutaneous, For Pain Relief

    FDA classification
    FDA Class 2 ·Stimulator, Nerve, Transcutaneous, For Pain Relief