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510(k) Data Aggregation

    K Number
    K102837
    Manufacturer
    Date Cleared
    2010-12-23

    (85 days)

    Product Code
    Regulation Number
    890.3900
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    HIROLLER ELEVATING WHEELCHAIR

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

    The HiRoller Elevating Wheelchair is a product that allows wheelchair users to raise and lower their seat height while seated in the wheelchair.

    Device Description

    Not Found

    AI/ML Overview

    The provided document is a 510(k) clearance letter from the FDA for a medical device called the "HiRoller Elevating Wheelchair." This type of document declares substantial equivalence to a predicate device, which means the new device is as safe and effective as a legally marketed device. It does not contain information about acceptance criteria or a study proving the device meets specific performance criteria in the way a clinical trial or performance study for an AI/CADe device would.

    Therefore, I cannot provide the detailed information requested in the prompt based on this document. The usual criteria like sensitivity, specificity, AUC, human reader improvement with AI, ground truth establishment, or training set size are not applicable to this type of regulatory submission for a physical medical device.

    Specifically, the following cannot be extracted from this 510(k) clearance letter:

    1. A table of acceptance criteria and the reported device performance: This document does not specify performance metrics or acceptance criteria for the HiRoller Elevating Wheelchair beyond its general intended use.
    2. Sample size used for the test set and the data provenance: Not applicable.
    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts: Not applicable.
    4. Adjudication method for the test set: Not applicable.
    5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance: Not applicable, as this is a physical wheelchair, not an AI/CADe device.
    6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done: Not applicable.
    7. The type of ground truth used (expert consensus, pathology, outcomes data, etc.): Not applicable.
    8. The sample size for the training set: Not applicable.
    9. How the ground truth for the training set was established: Not applicable.

    The document's purpose is to confirm that the HiRoller Elevating Wheelchair is substantially equivalent to a predicate device, allowing it to be marketed. This process primarily relies on demonstrating similar design, materials, and intended use as an already approved device, rather than explicit performance metrics from a study as would be seen for, for example, an AI diagnostic aid.

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