BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

    MUSMATE WALKING AID

    K Number: K073521 · Decision Feb 4, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    74
    Registration Numbers
    74
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    52

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    Basic Information

    Device Name
    MUSMATE WALKING AID
    K Number
    K073521
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.3475
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Musmate, Ltd.
    Date Received
    December 14, 2007
    Decision Date
    February 4, 2008
    Product Code
    OHI
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    OHI Orthosis, Foot Drop