BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    aprevo® anterior lumbar interbody fusion device with interfixation

    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

    Patient Monitoring Cables

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KINETIS Total Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Cable, Transducer And Electrode, Patient, (Including Connector)

    FDA classification
    FDA Class 2 ·Cable, Transducer And Electrode, Patient, (Including Connector)

    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

    FDA classification
    FDA Class 2 ·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer