BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

    SOFAMOR ORFIL SPINE FIXATION SYSTEM

    K Number: K934007 · Decision Jun 2, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    321
    Registration Numbers
    321
    Same Product Code
    429
    Applicant Total
    5
    Review Days
    288

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    Basic Information

    Device Name
    SOFAMOR ORFIL SPINE FIXATION SYSTEM
    K Number
    K934007
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3050
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Sofamor Co.
    Date Received
    August 18, 1993
    Decision Date
    June 2, 1994
    Product Code
    KWP
    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
    KWP Appliance, Fixation, Spinal Interlaminal

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