BEUDAMED
    4 results · 22ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    Heli-FX EndoAnchor System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endovascular Suturing System

    FDA classification
    FDA Class 2 ·Endovascular Suturing System

    CUTTING EDGE SPINE INTERBODY FUSION DEVICE

    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