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510(k) Data Aggregation

    K Number
    K991434
    Date Cleared
    1999-07-06

    (71 days)

    Product Code
    Regulation Number
    892.1000
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Magnetic resonance imaging (MRI) of the hand and wrist.

    Device Description

    Model 445PH-64 Quadrature Wrist Coil. Compatible with Philips Gyroscan ACS-NT 1.5T MRI system.

    AI/ML Overview

    This document describes the 510(k) summary for the Medical Advances, Inc. Model 445PH-64 Quadrature Wrist Coil, submitted on April 21, 1999 (K991434). This device is a Magnetic Resonance Imaging (MRI) coil intended for diagnostic imaging of the hand and wrist.

    1. Table of Acceptance Criteria and Reported Device Performance

    The acceptance criteria in this submission are framed around demonstrating substantial equivalence to the predicate device (the Philips Gyroscan ACS-NT 1.5T MRI system operated without the Medical Advances Quadrature Wrist Coil). The key performance parameters are assessed by showing "No change" compared to the predicate device, indicating that the addition of the new coil does not adversely affect these fundamental MRI system capabilities. No specific quantitative numerical acceptance thresholds are provided in this summary.

    Acceptance Criteria CategorySpecific ParameterReported Device Performance (with Medical Advances Quadrature Wrist Coil)
    Safety ParametersMaximum Static Magnetic FieldNo change
    Rate of Magnetic Field Strength ChangeNo change
    RF Power DepositionNo change
    Acoustic Noise LevelsNo change
    Imaging PerformanceSpecification VolumeNo change
    Signal-to-Noise RatioNo change
    Image UniformityNo change
    Geometric DistortionNo change
    Slice Thickness and GapNo change
    High Contrast Spatial ResolutionNo change
    General Safety and EffectivenessInstructions for Use (Indications, Precautions, Cautions, Contraindications, Warnings, QA Testing)Device includes these to assure safe and effective use.

    2. Sample Size Used for the Test Set and Data Provenance

    The provided 510(k) summary does not specify a separate "test set" in the context of clinical studies with human subjects or detailed performance evaluations for the Quadrature Wrist Coil. The submission relies on demonstrating that the new coil, when integrated with an existing, legally marketed MRI system (Philips Gyroscan ACS-NT 1.5T), does not alter the system's safety and imaging performance parameters.

    The data provenance is implied to be from engineering and technical testing of the coil's compatibility and performance characteristics within the specified MRI system, rather than a clinical study with patient data. No information on country of origin or whether it's retrospective/prospective is given, as it's not a clinical data-driven submission in the modern sense.

    3. Number of Experts Used to Establish the Ground Truth for the Test Set and Their Qualifications

    Given the nature of the submission, which focuses on demonstrating substantial equivalence through technical specifications rather than clinical diagnostic accuracy, no information is provided regarding experts used to establish ground truth for a test set. This type of submission does not involve a diagnostic accuracy study where ground truth would be established by medical experts for a set of cases.

    4. Adjudication Method for the Test Set

    As there is no specified test set involving human subject data or diagnostic interpretations, there is no mention of an adjudication method.

    5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study

    No MRMC comparative effectiveness study was performed by the device manufacturer, as this submission is for an MRI coil and focuses on technical equivalence rather than comparing diagnostic efficacy with and without AI assistance. The device itself is an accessory to an MRI system, not an AI-enabled diagnostic tool.

    6. Standalone (Algorithm Only) Performance Study

    No standalone performance study was done as the device is a passive MRI coil and does not incorporate an algorithm that operates independently.

    7. Type of Ground Truth Used

    The "ground truth" in this context is the established performance and safety specifications of the predicate Philips Gyroscan ACS-NT 1.5T MRI system when operating without the Medical Advances Quadrature Wrist Coil. The new coil is demonstrated to not alter these established parameters. This is based on technical specifications and engineering measurements rather than expert consensus, pathology, or outcomes data from a diagnostic study.

    8. Sample Size for the Training Set

    There is no mention of a training set as this device is a passive MRI coil and does not employ machine learning or AI algorithms requiring a training set.

    9. How the Ground Truth for the Training Set Was Established

    Since there is no training set, this question is not applicable.

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