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

    Ancora LLC Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Integrated Fixation, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Lumbar

    PARAMOUNT R IBF DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACS:180 AND ADVIA CENTAUR B-TYPE NATRIURETIC PEPTIDE (BNP) ASSAYS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Test, Natriuretic Peptide

    FDA classification
    FDA Class 2 ·Test, Natriuretic Peptide

    Intervertebral Fusion Device With Bone Graft, Lumbar

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