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

    LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002

    K Number: K082194 · Decision Aug 28, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    386
    Registration Numbers
    386
    Same Product Code
    680
    Applicant Total
    8
    Review Days
    24

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    Basic Information

    Device Name
    LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002
    K Number
    K082194
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.1100
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Laurimed, LLC
    Date Received
    August 4, 2008
    Decision Date
    August 28, 2008
    Product Code
    HRX
    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
    HRX Arthroscope

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