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

    PROFIX POSTERIOR-STABILIZED KNEE SYSTEM

    K Number: K954909 · Decision Jan 31, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    315
    Registration Numbers
    315
    Same Product Code
    910
    Applicant Total
    87
    Review Days
    98

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    Basic Information

    Device Name
    PROFIX POSTERIOR-STABILIZED KNEE SYSTEM
    K Number
    K954909
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3560
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent for Some Indications
    Applicant
    Smith & Nephew Richards, Inc.
    Date Received
    October 25, 1995
    Decision Date
    January 31, 1996
    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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