BEUDAMED
    4 results · 27ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    FRONTIER SADL INTERBODY FUSION DEVICE

    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

    VANGUARD REPROCESSED ENDOSCOPIC INSTRUMENTS

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

    Electrosurgical, Cutting & Coagulation & Accessories

    FDA classification
    FDA Class 2 ·Electrosurgical, Cutting & Coagulation & Accessories