BEUDAMED
    4 results · 21ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    SYNTHECEL DURA REPAIR, SYNTHECEL DURA ONLAY

    FDA 510(k)
    FDA Class 2 ·Neurology

    Dura Substitute

    FDA classification
    FDA Class 2 ·Dura Substitute

    MOBIS, MOVAL, SEMIAL, TETRISMODEL PEEK AND TITANIUM, KIMBA MODEL STANDARD AND MINI

    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