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

    NovaBone Putty - Bioactive Synthetic Bone Graft (NB6600, NB6610, NB6615)

    K Number: K240404 · Decision Mar 5, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    229
    Registration Numbers
    229
    Same Product Code
    491
    Applicant Total
    30
    Review Days
    25

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    Basic Information

    Device Name
    NovaBone Putty - Bioactive Synthetic Bone Graft (NB6600, NB6610, NB6615)
    K Number
    K240404
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3045
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Novabone Products, LLC
    Date Received
    February 9, 2024
    Decision Date
    March 5, 2024
    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 Novabone Products, LLC

    K Number Device Name
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