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

    INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OCTO

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Laparoscope, General & Plastic Surgery

    FDA classification
    FDA Class 2 ·Laparoscope, General & Plastic Surgery