BEUDAMED
    FDA Registration Active 🇺🇸 United States

    DBS Extension Kit

    Reg #: 2182207 · FEI: 2182207 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    11
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    MEDTRONIC NEUROMODULATION
    Registration Number
    2182207
    FEI Number
    2182207
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    7000 Central Ave., N.E.
    City
    Minneapolis
    State
    MN
    ZIP
    55432
    Country
    US

    Regulatory Submissions

    PMA Number
    H020007

    Owner / Operator

    Firm Name
    Medtronic, Inc.
    Operator Number
    2112641
    Address
    710 Medtronic Parkway
    City
    Minneapolis
    State
    MN
    Postal Code
    55432
    Country
    US

    Products

    Device Name Product Code
    Implanted Subcortical Electrical Stimulator (Motor Disorders) MRU
    Deep Brain Stimulator For Obsessive Compulsive Disorder (Ocd) OLM

    Proprietary Names

    DBS Extension Kit N'Vision Programmer N'Vision Software Application Card Activa Dystonia Therapy Activa SC Neurostimulator Activa PC Neurostimulator DBS Therapy for Dystonia Access Review Therapy Controller StimLoc Percept™ PC BrainSense™ SenSight™

    Establishment Types

    Manufacture Medical Device