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

    Normandy VBR System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Spinal Vertebral Body Replacement Device - Cervical

    FDA classification
    FDA Class 2 ·Spinal Vertebral Body Replacement Device - Cervical

    INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Electrode, Ion Specific, Sodium

    FDA classification
    FDA Class 2 ·Electrode, Ion Specific, Sodium

    Intervertebral Fusion Device With Bone Graft, Lumbar

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