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

    THE C-FIT & DC-FIT ACETABULAR CUP SYSTEM

    K Number: K972995 · Decision Nov 10, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    227
    Registration Numbers
    227
    Same Product Code
    562
    Applicant Total
    57
    Review Days
    90

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    Basic Information

    Device Name
    THE C-FIT & DC-FIT ACETABULAR CUP SYSTEM
    K Number
    K972995
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3350
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Corin USA
    Date Received
    August 12, 1997
    Decision Date
    November 10, 1997
    Product Code
    JDI
    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
    JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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