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

    NANOFUSE DBM

    K Number: K120279 · Decision Apr 6, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    229
    Registration Numbers
    229
    Same Product Code
    491
    Applicant Total
    2
    Review Days
    67

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    Basic Information

    Device Name
    NANOFUSE DBM
    K Number
    K120279
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3045
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Nanotherapeutics
    Date Received
    January 30, 2012
    Decision Date
    April 6, 2012
    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 Nanotherapeutics

    K Number Device Name
    K062459 ORIGEN DBM WITH BIOACTIVE GLASS