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

    DURACON MODULAR FEMORAL COMPONENT AND FEMORAL SPAC

    K Number: K920034 · Decision Mar 18, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    315
    Registration Numbers
    315
    Same Product Code
    910
    Applicant Total
    8
    Review Days
    72

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    Basic Information

    Device Name
    DURACON MODULAR FEMORAL COMPONENT AND FEMORAL SPAC
    K Number
    K920034
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3560
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Pfizer Hospital Products Group, Inc.
    Date Received
    January 6, 1992
    Decision Date
    March 18, 1992
    Product Code
    JWH
    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
    JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

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