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

    Intracept Intraosseous Nerve Ablation System

    FDA 510(k)
    FDA Class 2 ·Neurology

    Probe, Radiofrequency Lesion

    FDA classification
    FDA Class 2 ·Probe, Radiofrequency Lesion

    QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN

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

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA classification
    FDA Class 2 ·Suture, Absorbable, Synthetic, Polyglycolic Acid