BEUDAMED
    FDA Registration Active 🇺🇸 United States

    screening cable

    Reg #: 2182207 · FEI: 2182207 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    2
    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

    510(k) Number
    K960631

    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
    Stimulator, Spinal-Cord, Implanted (Pain Relief) GZB
    Stimulator, Peripheral Nerve, Implanted (Pain Relief) GZF

    Proprietary Names

    screening cable accessory kit

    Establishment Types

    Manufacture Medical Device