BEUDAMED
    4 results · 21ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    PIONEER SPINOUS PROCESS FUSION PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PERIMETER INTERBODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Appliance, Fixation, Spinal Interlaminal

    FDA classification
    FDA Class 2 ·Appliance, Fixation, Spinal Interlaminal

    Intervertebral Fusion Device With Bone Graft, Lumbar

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