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510(k) Data Aggregation

    K Number
    K193207
    Device Name
    TaiChiA
    Date Cleared
    2020-08-07

    (261 days)

    Product Code
    Regulation Number
    892.5050
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K171733

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

    TaiChiA, is a Medical Linear Accelerator intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body where radiation treatment is indicated.

    Device Description

    TaiChiA Medical Linear Accelerator, has been designed to deliver radiation treatment in accordance with a prescribed plan. This system utilizes kV image guidance technology (IGRT) to deliver photon based radiation therapy treatments, using an integrated rotating linear accelerator system. TaiChiA is a single energy medical linear accelerator designed to deliver Image Guided Radiation Therapy and Radiosurgery, using 3DCRT, IMRT and VMAT techniques. It consists of the accelerator and patient support within a radiation shielded treatment room and a control console in the control room.

    AI/ML Overview

    The provided text does not contain explicit acceptance criteria and device performance in a table format, nor does it detail a study proving the device meets specific acceptance criteria using statistical measures (sensitivity, specificity, etc.) typically associated with AI/ML performance. The document describes a medical linear accelerator (TaiChiA) and compares its specifications to predicate and reference devices in tables, asserting substantial equivalence. It confirms various verification and validation tests were performed (electrical safety, EMC, bench tests, hardware/software) to show compliance with relevant standards and specifications.

    However, based on the provided text, I can extract and infer information about the device's specifications and the type of testing performed for its regulatory clearance.

    Here's a breakdown of the requested information based on the provided document:

    1. Table of Acceptance Criteria and Reported Device Performance

    The document does not provide a formal table of "acceptance criteria" against which specific "device performance" metrics (like accuracy, sensitivity, specificity for an AI component) are reported. Instead, it presents detailed comparative tables of the TaiChiA's specifications against a predicate device (Varian Halcyon, K181032) and a reference device (Varian TrueBeam, K171733). The "acceptance criteria" here are implicitly the demonstrated equivalence or comparable performance to these legally marketed devices across various physical and functional attributes. The "reported device performance" is the TaiChiA's specifications as listed in these comparison tables.

    Below is a summary of key comparative specifications. These essentially serve as the "performance" metrics evaluated for substantial equivalence.

    Attribute/FeaturePredicate Device (Varian Halcyon, K181032)Proposed Device (TaiChiA Medical Linear Accelerator)Reference Device (TrueBeam, K171733)
    Beam Specification
    Beam energy (MV)6MV, FFF6MV, FFF6/8/10/15/18/20MV (FF), 6/10MV (FFF). (TaiChiA 6MV FFF)
    Maximum dose rate (cGy/min)Up to 800Up to 1400Up to 1400 (6MV FFF)
    Maximum treatment field (cm)28x2840x4040x40
    Dmax (cm)1.3 +/- 0.21.5 +/- 0.2Not explicitly listed in TrueBeam comparison
    Percentage dose at 10 cm depth (%)63.0 +/- 1.065.0 +/- 2.0Not explicitly listed in TrueBeam comparison
    Off axis intensity (%)79.0 +/- 2.076.0 +/- 2.0Not explicitly listed in TrueBeam comparison
    Symmetry (%)
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