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

    MCCAIN INSTRUMENT TMJ/SM. JOINT ARTHROSCOPIC SURG

    K Number: K874911 · Decision Feb 24, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    386
    Registration Numbers
    386
    Same Product Code
    680
    Applicant Total
    56
    Review Days
    84

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    Basic Information

    Device Name
    MCCAIN INSTRUMENT TMJ/SM. JOINT ARTHROSCOPIC SURG
    K Number
    K874911
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.1100
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Applicant
    Walter Lorenz Surgical, Inc.
    Date Received
    December 2, 1987
    Decision Date
    February 24, 1988
    Product Code
    HRX
    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
    HRX Arthroscope

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