BEUDAMED
    4 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    VERSAVIT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    VU C*POD INTERVERTEBRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Instrument, Vitreous Aspiration And Cutting, Ac-Powered

    FDA classification
    FDA Class 2 ·Instrument, Vitreous Aspiration And Cutting, Ac-Powered

    Intervertebral Fusion Device With Bone Graft, Cervical

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