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

    TOGGLELOC AND JUGGERLOC IMPLANTS/INSTRUMENTS/KITS

    K Number: K141263 · Decision Nov 19, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    245
    Registration Numbers
    245
    Same Product Code
    230
    Applicant Total
    93
    Review Days
    188

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    Basic Information

    Device Name
    TOGGLELOC AND JUGGERLOC IMPLANTS/INSTRUMENTS/KITS
    K Number
    K141263
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3030
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Biomet Manufacturing Corp
    Date Received
    May 15, 2014
    Decision Date
    November 19, 2014
    Product Code
    JDR
    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
    JDR Staple, Fixation, Bone

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