BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODULAR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SURGICAL LIGHTSTIC 180, MODEL 180 L, MODEL 180 C

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

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

    FDA classification
    FDA Class 2 ·Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

    Gas-Machine, Anesthesia

    FDA classification
    FDA Class 2 ·Gas-Machine, Anesthesia