BEUDAMED
    179 results · 29ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    ASK-300

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ASK System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NERVEL-NERVE CONDUCTION VELOCITY METER

    FDA 510(k)
    FDA Class 2 ·Neurology

    FIRM MASTER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    AccuPoint Electrode

    FDA 510(k)
    FDA Class 2 ·Neurology

    Synvitro Hyadase

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/PROXIMITY(TM) INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE

    BAK-ON SP PORCELAIN ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) (R) INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/L INTERBODY FUSION SYSTEM

    MODIFICATION TO BONE ANCHOR AND KIT (BAK)

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

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM