BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Pump, Infusion, Implanted, Programmable

    PMA: P890055 · Supplement: S033 · Decision May 23, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18

    Basic Information

    Device Name
    Pump, Infusion, Implanted, Programmable
    Trade Name
    MEDSTREAM PROGRAMMABLE INFUSION SYSTEM
    PMA Number
    P890055
    Supplement Number
    S033
    Device Class
    FDA Class 3
    Product Code
    LKK
    Generic Name
    Pump, infusion, implanted, programmable
    Medical Specialty
    Unknown
    Advisory Committee
    General Hospital
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    May 23, 2011
    Date Received
    January 28, 2011
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR SOFTWARE MODIFICATION TO THE MEDSTREAM PROGRAMMABLE INFUSION SYSTEM. THE MODIFIED MEDSTREAM PUMP WILL HAVE SOFTWARE PS-100044 VERSION 3.06, THE MODIFIED CONTROL UNIT WILL HAVE SOFTWARE PS-100046 VERSION 3.00. PS-100045 VERSION 3.04, PS-1000047 VERSION 3.09 AND PS-100021 VERSION 2.00. THE DEVICE,AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME MEDSTREAM PROGRAMMABLE INFUSION SYSTEM AND IS INDICATED FOR THE CHRONIC INTRATHECAL INFUSION OF BACLOFEN INJECTION STERILE SOLUTION (5.0 PH TO 7.0PH) IN THE TREATMENT OF SEVERE SPASTICITY.

    Classifications

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

    Product Code Device Name
    LKK Pump, Infusion, Implanted, Programmable