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

    Internal Distraction - Sterile

    K Number: K161470 · Decision Dec 1, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    30
    Registration Numbers
    30
    Same Product Code
    59
    Applicant Total
    20
    Review Days
    188

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    Basic Information

    Device Name
    Internal Distraction - Sterile
    K Number
    K161470
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.4760
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    KLS Martin L.P.
    Date Received
    May 27, 2016
    Decision Date
    December 1, 2016
    Product Code
    MQN
    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
    MQN External Mandibular Fixator And/Or Distractor

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