BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

    LIGAFIX INTERFERENCE SCREW

    K Number: K061262 · Decision Jul 5, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    659
    Registration Numbers
    659
    Same Product Code
    1058
    Applicant Total
    2
    Review Days
    61

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    Basic Information

    Device Name
    LIGAFIX INTERFERENCE SCREW
    K Number
    K061262
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3040
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sciences For Bio Materials
    Date Received
    May 5, 2006
    Decision Date
    July 5, 2006
    Product Code
    HWC
    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
    HWC Screw, Fixation, Bone

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    Other Clearances by Sciences For Bio Materials

    K Number Device Name
    K050407 LIGAFIX RESORBABLE INTERFERENCE SCREW, MODELS 30 AND 60