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510(k) Data Aggregation

    K Number
    K091114
    Date Cleared
    2009-05-01

    (14 days)

    Product Code
    Regulation Number
    892.1000
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K021262, K021330

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

    For use with a 1.5T Siemens Avanto/Espree or 3T Siemens Trio a TIM/Verio magnetic resonance scanner to produce diagnostic images of the head that can be interpreted by a trained physician.

    Device Description

    The 1.5T and 3T CP Head Coils are circularly polarized (CP) transmit and receive coils designed for magnetic resonance imaging of the head. The coils are designed for use with the Siemens MAGNETOM 1.5T Avanto/Espree and Siemens MAGNETOM 3T Trio a TIM/Verio systems respectively. The coil elements are enclosed in a rigid plastic housing (polycarbonate) which is fire-rated and has impact and tensile strength (material data provided). The coils have a split-top mechanical design with a system cable on the posterior half of the coil. The inner cross section is shaped to fit the head anatomy. The coils include the following accessories: a mirror to reduce patient anxiety/claustrophobia and foam pads also to aid positioning and enhance patient comfort.

    AI/ML Overview

    This submission (K091114) is for an MRI head coil, specifically the TxRx 1.5T CP Head Coil and TxRx 3T CP Head Coil, and not for an AI/ML device. Therefore, the provided document does not contain information regarding various aspects typically associated with AI/ML device evaluations. As such the questions are not applicable to the provided document.

    Here's why and what information is available in the document:

    Why the questions are not applicable (and the information is missing):

    • No AI/ML Device: The device is a magnetic resonance (MR) head coil, a hardware component for MRI scanners. It does not perform any Al/ML functions like image interpretation, anomaly detection, or diagnostic assistance.
    • No 'Performance' in the AI/ML Sense: The "performance" of an MR coil is typically evaluated based on signal-to-noise ratio, image uniformity, specific absorption rate (SAR), and other physical/electrical characteristics, not diagnostic accuracy metrics (like sensitivity, specificity, AUC) that would be established against a medical ground truth.
    • No Clinical Study for Diagnostic Efficacy: The 510(k) summary indicates substantial equivalence to predicate devices (other MR head coils). This usually means that the new device performs similarly in terms of image quality and safety, and does not require a new clinical study demonstrating diagnostic performance against a ground truth.

    Information that is available from the document:

    • Device Description: The TxRx 1.5T and 3T CP Head Coils are circularly polarized transmit and receive coils designed for magnetic resonance imaging of the head. They are intended for use with specific Siemens MAGNETOM 1.5T Avanto/Espree and 3T Trio a TIM/Verio MRI systems, respectively.
    • Intended Use: "For use with a 1.5T Siemens Avanto/Espree or 3T Siemens Trio a TIM/Verio magnetic resonance scanner to produce diagnostic images of the head that can be interpreted by a trained physician."
    • Substantial Equivalence: The submission concludes that the new coils are substantially equivalent to legally marketed predicate devices (MAGNETOM Symphony Head Coil and MAGNETOM Trio Head Coil from USA Instruments) because they have similar designs, are constructed of similar materials, and their use does not result in any new potential hazards.

    Therefore, I cannot provide answers to the questions because the provided document does not pertain to an AI/ML device or a study evaluating diagnostic performance against a ground truth.

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