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

    SMOOTH STAPLE IMPLANT

    K Number: K900433 · Decision Nov 16, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    1
    Applicant Total
    1
    Review Days
    290

    Basic Information

    Device Name
    SMOOTH STAPLE IMPLANT
    K Number
    K900433
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.4760
    Medical Specialty
    Dental
    Decision
    Unknown
    Applicant
    INTERPHASE IMPLANTS, INC.
    Date Received
    January 30, 1990
    Decision Date
    November 16, 1990
    Product Code
    MDL
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MDL Implant, Transmandibular

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