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510(k) Data Aggregation

    K Number
    K031725
    Manufacturer
    Date Cleared
    2003-06-24

    (21 days)

    Product Code
    Regulation Number
    888.3030
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    SYNTHES TI-15 MO LOCKING DISTAL RADIUS PLATING SYSTEM

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

    The Synthes Ti-15Mo Locking Distal Radius Plating System is intended for fixation of complex intra- and extra-articular fractures and osteotomies of the distal radius and other small bones.

    Device Description

    The Synthes Ti-15Mo Locking Distal Radius Plating System consists of machined metallic plates and screws that offer screw to plate locking designed for various fracture modes of the distal end of the radius.

    AI/ML Overview

    The provided text is a 510(k) summary for the Synthes Ti-15Mo Locking Distal Radius Plating System. This document focuses on demonstrating substantial equivalence to a predicate device rather than presenting a study proving a device meets specific performance-based acceptance criteria for AI/ML-enabled software.

    Therefore, this document does not contain the information requested in the prompt regarding acceptance criteria and performance studies for an AI/ML device. The device described is a physical implant (bone plate and screws), not a software or AI/ML product.

    Here's why the requested information is absent:

    • Acceptance Criteria and Performance: The document aims to establish that the new device is as safe and effective as a previously marketed predicate device. It doesn't define quantitative performance acceptance criteria or report performance against such criteria.
    • Sample Sizes (Test/Training Data), Data Provenance, Experts, Adjudication, MRMC, Standalone Performance, Ground Truth: These are all concepts relevant to the validation of AI/ML algorithms using clinical data. A physical implant like a bone plate does not undergo these types of studies for 510(k) clearance. Its equivalence is typically based on material properties, design, and intended use compared to the predicate.

    In summary, the provided text describes a medical device, but it is not an AI/ML device, and thus the requested information regarding acceptance criteria and studies for AI/ML performance is not present.

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