BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    restor3d TiDAL Lumbar Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Biolign® Roto-Loc Cervical Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Allergen And Vaccine Delivery Needles

    FDA classification
    FDA Class 2 ·Allergen And Vaccine Delivery Needles

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Appliance, Fixation, Spinal Intervertebral Body

    FDA classification
    FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body