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

    aprevo® anterior and lateral lumbar interbody fusion devices, aprevo® transforaminal lumbar interbody fusion devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Picore

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Powered Laser Surgical Instrument

    FDA classification
    FDA Class 2 ·Powered Laser Surgical Instrument