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

    MiRus™ Lumbar Interbody Fusion System consisting of CALLISTO™ PEEK Posterior Lumbar Interbody Fusion (PLIF); HYPERION™ PEEK Transforaminal Lumbar Interbody Fusion (TLIF); CALPYSO™ PEEK Lateral Lumbar Interbody Fusion (LLIF); ANTARES™ PEEK Anterior Lumbar Interbody Fusion (ALIF)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELECTRONIC BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RANGE SPINAL SYSTEM (MESA AND DENALI)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Orthosis, Spinal Pedicle Fixation

    FDA classification
    FDA Class 2 ·Orthosis, Spinal Pedicle Fixation

    System, Measurement, Blood-Pressure, Non-Invasive

    FDA classification
    FDA Class 2 ·System, Measurement, Blood-Pressure, Non-Invasive