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

    PRECISION SPINAL ADJUSTER MODEL 115

    K Number: K870910 · Decision Apr 26, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    31
    Applicant Total
    5
    Review Days
    418

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    Basic Information

    Device Name
    PRECISION SPINAL ADJUSTER MODEL 115
    K Number
    K870910
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Kinetic Technology, Inc.
    Date Received
    March 5, 1987
    Decision Date
    April 26, 1988
    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
    K922692 KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR
    K922695 KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5
    K922693 KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1
    K922694 KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4