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

    Lumbar Interbody Fusion System (ALIF, PLIF, LLIF, TPLIF)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CONTOUR EMBOLIZATION PARTICLES, MODELS M0017600121, M0017600221, M0017600321

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PAIRETEX OPTIMIZED COMPOSITE MESH (PCO-FX REFRENCES)

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

    Agents, Embolic, For Treatment Of Uterine Fibroids

    FDA classification
    FDA Class 2 ·Agents, Embolic, For Treatment Of Uterine Fibroids

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Mesh, Surgical, Polymeric

    FDA classification
    FDA Class 2 ·Mesh, Surgical, Polymeric