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

    CARRICELL

    K Number: K132868 · Decision Feb 20, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    229
    Registration Numbers
    229
    Same Product Code
    491
    Applicant Total
    5
    Review Days
    525

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    Basic Information

    Device Name
    CARRICELL
    K Number
    K132868
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3045
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Etex Corporation
    Date Received
    September 13, 2013
    Decision Date
    February 20, 2015
    Product Code
    MQV
    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
    MQV Filler, Bone Void, Calcium Compound

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    Other Clearances by Etex Corporation

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    K141245 ETEX MIXING AND DELIVERY SYSTEM
    K102812 GAMMA-BSM; BETA-BSM; EQUIVABONE