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

    OTI EUROPEAN COMPRESSION SYSTEM

    K Number: K925571 · Decision Jul 13, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    519
    Registration Numbers
    519
    Same Product Code
    1313
    Applicant Total
    3
    Review Days
    252

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    Basic Information

    Device Name
    OTI EUROPEAN COMPRESSION SYSTEM
    K Number
    K925571
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3030
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Osteo-Technology Intl., Inc.
    Date Received
    November 3, 1992
    Decision Date
    July 13, 1993
    Product Code
    HRS
    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
    HRS Plate, Fixation, Bone

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    Other Clearances by Osteo-Technology Intl., Inc.

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