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

    Duo™ Lumbar Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPY ANALYSIS TOOLKIT, MODEL SA9000

    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, Image Processing, Radiological

    FDA classification
    FDA Class 2 ·System, Image Processing, Radiological