BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    Curiteva Porous PEEK Cervical Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINEOLOGY PEEK BULLET LUMBAR INTERBODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMPRESSOR NEBULIZER MODEL MCN-S600XX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Intervertebral Fusion Device With Bone Graft, Cervical

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

    Nebulizer (Direct Patient Interface)

    FDA classification
    FDA Class 2 ·Nebulizer (Direct Patient Interface)

    Intervertebral Fusion Device With Bone Graft, Lumbar

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