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

    KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR

    K Number: K922692 · Decision Sep 30, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    31
    Applicant Total
    5
    Review Days
    118

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    Basic Information

    Device Name
    KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR
    K Number
    K922692
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Kinetic Technology, Inc.
    Date Received
    June 4, 1992
    Decision Date
    September 30, 1992
    Product Code
    LXM
    Advisory Committee
    Unknown
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LXM Manipulator, Plunger-Like Joint

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    Other Clearances by Kinetic Technology, Inc.

    K Number Device Name
    K922695 KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5
    K922693 KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1
    K922694 KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4
    K870910 PRECISION SPINAL ADJUSTER MODEL 115