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510(k) Data Aggregation

    K Number
    K970658
    Date Cleared
    1997-05-19

    (87 days)

    Product Code
    Regulation Number
    882.5550
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    LUMBAR DRAINAGE ACCESSORY KIT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The major indication of external drainage is the management of hydrocephalic shunt infections. External drainage of cerebrospinal fluid (CSF) to control increased intercranial pressure may also be indicated if an internal shunt is not indicated or during the treatment of other cerebral conditions such as pre-operative drainage, intraventricular hemorrhage and post-operative pressure monitoring. This device should only be used by a physician or qualified personnel under the direction of a physician.

    Device Description

    Lumbar Drainage Accessory Kit

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for a device called "Lumbar Drainage Accessory Kit". It does not contain any information about acceptance criteria, device performance metrics, study designs, sample sizes (training or test sets), expert qualifications, ground truth establishment, or multi-reader multi-case studies.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets the acceptance criteria based on the provided input.

    The document primarily focuses on the FDA's determination of substantial equivalence for the device to previously marketed devices and outlines regulatory responsibilities. Section 8 ("DEVICE INDICATIONS FOR USE") describes the intended uses of the device but does not include any performance data or study details.

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