BEUDAMED
    FDA 510(k) FDA class 3 Substantially Equivalent for Some Indications 🇺🇸 United States

    POROUS-COATED TITANIUM ACETABULAR CUP

    K Number: K894965 · Decision Nov 17, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    50
    Registration Numbers
    50
    Same Product Code
    44
    Applicant Total
    74
    Review Days
    102

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    Basic Information

    Device Name
    POROUS-COATED TITANIUM ACETABULAR CUP
    K Number
    K894965
    Device Class
    FDA class 3
    Clearance Type
    Traditional
    Regulation Number
    888.3320
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent for Some Indications
    Applicant
    Dow Corning Wright
    Date Received
    August 7, 1989
    Decision Date
    November 17, 1989
    Product Code
    JDL
    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
    JDL Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)

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