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

    RIOPRO COBALT TRAPEZIOMETARCARPAL RESURFACING COMPONENT

    K Number: K964472 · Decision Feb 3, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    21
    Registration Numbers
    21
    Same Product Code
    25
    Applicant Total
    9
    Review Days
    88

    Basic Information

    Device Name
    RIOPRO COBALT TRAPEZIOMETARCARPAL RESURFACING COMPONENT
    K Number
    K964472
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3770
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    BIOLOGICALLY ORIENTED PROSTHESES
    Date Received
    November 7, 1996
    Decision Date
    February 3, 1997
    Product Code
    KYI
    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
    KYI Prosthesis, Wrist, Carpal Trapezium

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