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

    VECTOR TARGETING SYSTEM

    K Number: K001938 · Decision Aug 29, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    302
    Registration Numbers
    302
    Same Product Code
    528
    Applicant Total
    2
    Review Days
    64

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    Basic Information

    Device Name
    VECTOR TARGETING SYSTEM
    K Number
    K001938
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3020
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Vector Medical, Inc.
    Date Received
    June 26, 2000
    Decision Date
    August 29, 2000
    Product Code
    HSB
    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
    HSB Rod, Fixation, Intramedullary And Accessories

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    Other Clearances by Vector Medical, Inc.

    K Number Device Name
    K022225 VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM