BEUDAMED
    10 results · 8ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Fda510k × Classification: FDA Class 2 × Clear all

    VERIGENE C. DIFFICILE NUCLEIC ACID TEST (CDF)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF

    FDA 510(k)
    FDA Class 2 ·Neurology

    Alta ACDF System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ProAM ACDF System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X NO CAM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PATRIOT SPACERS: COLONIAL ACDF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNiTi ACDF Implant System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TotalTi ACDF by SAGICO

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    aprevo® anterior lumbar interbody fusion device; aprevo® lateral lumbar interbody fusion device; aprevo® anterior lumbar interbody fusion device with interfixation; aprevo® transforaminal lumbar interbody fusion device; aprevo® TLIF-CA Articulating System; aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X No Cams

    FDA 510(k)
    FDA Class 2 ·Orthopedic