BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    PMA: P010032 · Supplement: S186 · Decision Dec 16, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    55
    Registration Numbers
    55

    Basic Information

    Device Name
    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
    Trade Name
    Eterna SCS IPG, Charger, Patient Controller Application, Clinician Programmer Application
    PMA Number
    P010032
    Supplement Number
    S186
    Device Class
    FDA Class 3
    Product Code
    LGW
    Generic Name
    Stimulator, spinal-cord, totally implanted for pain relief
    Medical Specialty
    Unknown
    Advisory Committee
    Neurology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    December 16, 2022
    Date Received
    April 1, 2022
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    Approval for approval for commercial distribution of Abbotts Eterna Spinal Cord Stimulation (SCS) System. This system consists of a rechargeable Implantable Pulse Generator (IPG), Charging System, and Clinician Programmer Application and Patient Controller Application. These components are intended to be used with commercially available SCS leads, extensions and accessories.

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LGW Stimulator, Spinal-Cord, Totally Implanted For Pain Relief