BEUDAMED
    FDA 510(k) FDA class 2 Unknown 🇨🇭 Switzerland

    D-C-S SYSTEM

    K Number: K930657 · Decision Jun 29, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    321
    Registration Numbers
    321
    Same Product Code
    429
    Applicant Total
    1
    Review Days
    505

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    Basic Information

    Device Name
    D-C-S SYSTEM
    K Number
    K930657
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3050
    Medical Specialty
    Orthopedic
    Decision
    Unknown
    Statement or Summary
    Summary
    Applicant
    Pina-Vertriebs
    Date Received
    February 9, 1993
    Decision Date
    June 29, 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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