BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RHIGENE MESACUP-2 TEST RNP, MODEL M7741

    FDA 510(k)
    FDA Class 2 ·Immunology

    VARISEED 7.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    Anti-Rnp Antibody, Antigen And Control

    FDA classification
    FDA Class 2 ·Anti-Rnp Antibody, Antigen And Control

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    System, Planning, Radiation Therapy Treatment

    FDA classification
    FDA Class 2 ·System, Planning, Radiation Therapy Treatment