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

    COROENT XL-F SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Integrated Fixation, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Lumbar

    PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Cement, Bone, Vertebroplasty

    FDA classification
    FDA Class 2 ·Cement, Bone, Vertebroplasty