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510(k) Data Aggregation

    K Number
    K130457
    Date Cleared
    2013-05-20

    (87 days)

    Product Code
    Regulation Number
    892.1000
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    3T DISTAL COIL, 3T ELBOW COIL, 3T LONG BONE COIL

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

    The intended use for the device family is to provide form fitting MRI antenna sets to facilitate targeting imaging of various musculoskeletal extremity regions using a GE 3.0T MRI scanner. The Indications for use are:

    • Soft tissue and bone imaging of the extremities as allowed by the MRI system. .
    • Magnetic resonance peripheral angiography.
    Device Description

    The individual coils that comprise the Extremity Coil Family interface with a 3.0 Tesla, 8channel MRI scanner.
    All coils included in the Extremity Set are extremely similar in design, construction, materials and operation. There are slight variations in physical size (to accommodate differing patient sizes), and slight physical housing variations (required to optimize the image quality depending on the extremity anatomy). The designs and matcrials used to manufacture the individual coils are nearly identical and are no different from standard MRI coil technology that has existed for years. The geometry of each coil housing has been formed by utilizing a semi-rigid housing in conjunction with semi-flexible flaps and/or padding that facilitates close coupling of the imaging coil's region-of-sensitivity to the anatomy of interest on a broad size variation of patient anatomy. All employ similar blocking, impedance matching and integrated pre-amplifier circuitry.

    AI/ML Overview

    The provided text is a 510(k) summary for the Extremity Coil Family, which describes MRI coils. This type of document is for a medical device that serves as an accessory to an imaging system (MR scanner). It focuses on establishing substantial equivalence to a predicate device, rather than proving the performance of a diagnostic algorithm or AI.

    Therefore, the information requested regarding acceptance criteria, device performance, sample sizes, ground truth establishment, expert qualifications, and comparative effectiveness with AI is not applicable to this submission. These coils are hardware components whose performance is typically evaluated based on engineering specifications related to signal-to-noise ratio (SNR), image uniformity, and physical compatibility with the MRI scanner.

    The document confirms that this device is a basic MRI coil, not an AI-driven diagnostic tool. It states: "The designs and materials used to manufacture the individual coils are nearly identical and are no different from standard MRI coil technology that has existed for years."

    No study related to AI or diagnostic performance is mentioned in the provided text.

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