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

    SIRION Lateral Lumbar Interbody Fusion

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    M3290B INTELLIVUE INFORMATION CENTER SOFTWARE, RELEASE A.0

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

    FDA classification
    FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

    Intervertebral Fusion Device With Bone Graft, Lumbar

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