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510(k) Data Aggregation

    K Number
    K200704
    Device Name
    ZedView
    Manufacturer
    Date Cleared
    2021-05-27

    (435 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    ZedView is indicated for pre-operative planning and post-operative evaluations for various surgical procedures such as artificial joint replacement (arthroplasty), osteotomy, trauma, deformity correction.

    Device Description

    ZedView is a software package that provides computer-assisted 3D planning and evaluations using 2D image data in DICOM or other formats, for various pre-operative surgical procedures and post-operative evaluations. The software is composed of various modules described below.

    AI/ML Overview

    The provided text is a 510(k) summary for ZedView ver.14.0. It defines the device, its intended use, and compares it to a predicate device. However, it does not contain any information about acceptance criteria or a study that proves the device meets specific performance metrics, especially in the context of an AI/ML device.

    The document explicitly states: "6.8 Clinical Performance Test Summary: None." This indicates that no clinical performance tests (which would typically involve evaluating the device against acceptance criteria) were performed or submitted.

    The submission focuses on demonstrating substantial equivalence based on similar device specifications, operational principles, technical characteristics, and intended use as its predicate device, ZedView (K133022), rather than providing performance data against specific acceptance criteria.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets the acceptance criteria, as this information is not present in the provided document.

    If this were a different type of submission (e.g., a De Novo request for a novel AI/ML device), or if the 510(k) summary had included detailed performance testing, then such information would be available.

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