BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    PROVIDENCE MOLDING HELMET

    K Number: K030669 · Decision Jul 18, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    16
    Registration Numbers
    16
    Same Product Code
    42
    Applicant Total
    1
    Review Days
    137

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    Basic Information

    Device Name
    PROVIDENCE MOLDING HELMET
    K Number
    K030669
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    882.5970
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Northeast Orthotics and Prothetics, Inc.
    Date Received
    March 3, 2003
    Decision Date
    July 18, 2003
    Product Code
    MVA
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MVA Orthosis, Cranial

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