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510(k) Data Aggregation

    K Number
    K180815
    Manufacturer
    Date Cleared
    2018-06-22

    (85 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    MIM - SPECTRA Quant

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

    MIM software is used by trained medical professionals as a tool to aid in evaluation and information management of digital medical images. The medical image modalities include, but are not limited to, CT. MRI. CR. DX. MG. US. SPECT. PET and XA as supported by ACRNEMA DICOM 3.0. MIM assists in the following indications:

    • · Receive, transmit, store, retrieve, display, print, and process medical images and DICOM objects.
    • · Create, display and print reports from medical images.
    • · Registration, fusion display, and review of medical images for diagnosis, treatment planning,
      · Evaluation of cardiac left ventricular function, including left ventricular end-diastolic volume, end-systolic volume, and ejection fraction.
      · Localization and definition of objects such as tumors and normal tissues in medical images.
      · Creation, transformation, and modification of contours for applications including, but not limited to, quantitative analysis, aiding adaptive therapy, transfering contours to radiation therapy treatment planning systems, and archiving contours for patient follow-up and management.
      · Quantitative and statistical analysis of PET/SPECT brain scans by comparing to other registered PET/SPECT brain scans.
      · Planning and evaluation of permanent implant brachytherapy procedures (not including radioactive microspheres).
    • · Post-treatment dose calculation of permanent Yttrium-90 (Y90) microsphere implants.
      Lossy compressed mammographic images and digitized film screen images must not be reviewed for primary image interpretations. Images that are printed to film must be printed using a FDA-approved printer for the diagnosis of digital mammography images. Mammographic images must be viewed on a display system that has been cleared by the FDA for the diagnosis of digital mammography images.

    The software is not to be used for mammography CAD.

    Device Description

    MIM - SPECTRA Quant is a feature of MIM. It is designed for use in medical imaging and operates on both Windows and Mac computer systems. MIM - SPECTRA Quant extends the functionality MIM - Y90 Dosimetry (K172218) software. The following functions have been added to allow quantitative reconstructions of Single Photon Emission Computed Tomography (SPECT) scans:

    • Allows for decay correction of activity back to time of injection ●
    • Allows for correction of photon attenuation ●
    • . Allows for correction of photon scatter
    • Allows for correction of collimator detector resolution effects ●
    • Allows for camera sensitivity calibration providing output in Becquerels per ml (Bq/ml) .
    AI/ML Overview

    Here's a breakdown of the acceptance criteria and study details for MIM - SPECTRA Quant based on the provided document:


    1. Table of Acceptance Criteria and Reported Device Performance

    IsotopeCollimatorAcceptance Criteria (Quantitative Error)Reported Quantitative ErrorVerification Result
    Tc99mLEHR
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