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

    NORMED COMPRESSION BONE SCREW SYSTEM

    K Number: K032634 · Decision Oct 6, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    115
    Registration Numbers
    115
    Same Product Code
    52
    Applicant Total
    2
    Review Days
    41

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    Basic Information

    Device Name
    NORMED COMPRESSION BONE SCREW SYSTEM
    K Number
    K032634
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3030
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Noviace Corporation
    Date Received
    August 26, 2003
    Decision Date
    October 6, 2003
    Product Code
    JDS
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JDS Nail, Fixation, Bone

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