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510(k) Data Aggregation

    K Number
    K152283

    Validate with FDA (Live)

    Device Name
    MAGNETOM Amira
    Date Cleared
    2015-12-24

    (134 days)

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

    MAGNETOM Amira is indicated for use as a magnetic resonance diagnostic device (MRDD) that produces transverse, sagittal, coronal and oblique cross sectional images, spectroscopic images and/or spectra, and that displays the internal structure and/or function of the head, body, or extremities. Other physical parameters derived from the images and/or spectra may also be produced. Depending on the region of interest, contrast agents may be used.

    These images and or spectra and the physical parameters derived from the images and/or spectra when interpreted by a trained physician yield information that may assist in diagnosis.

    MAGNETOM Amira may also be used for imaging during interventional procedures when performed with MR compatible devices such as in-room displays and MR Safe biopsy needles.

    Device Description

    MAGNETOM Amira (1.5T) is an MRI svstem that is substantially equivalent to the previously cleared primary predicate device MAGNETOM Aera (K141977, cleared November 19, 2014) and secondary predicate device MAGNETOM ESSENZA (K130262, cleared Mach 1, 2013).

    The MAGNETOM Amira utilizes a superconducting magnet design. The open bore, whole body scanners are designed for increased patient comfort. They focus on ergonomics and usability to simplify the MR workflow.

    The MAGNETOM Amira systems will be available in a fixed configuration.

    AI/ML Overview

    This document describes the FDA 510(k) clearance for the Siemens MAGNETOM Amira with Software syngo MR E11, a magnetic resonance diagnostic device (MRDD). It does not contain information about acceptance criteria for an AI/ML powered device, nor does it detail a study proving such a device meets acceptance criteria.

    The document primarily focuses on demonstrating substantial equivalence to previously cleared predicate devices (MAGNETOM Aera and MAGNETOM ESSENZA) based on its intended use and technological characteristics, not on the performance of an AI-powered component.

    Therefore, I cannot extract the requested information regarding acceptance criteria, device performance, sample sizes, ground truth, or MRMC studies related to an AI component, as this information is not present in the provided text.

    The information provided pertains to the device itself (MAGNETOM Amira) as a magnetic resonance diagnostic device, and not to an AI/ML algorithm within or associated with it.

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