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510(k) Data Aggregation

    K Number
    K202762
    Date Cleared
    2020-11-16

    (56 days)

    Product Code
    Regulation Number
    888.3030
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    External fixation devices are used on adults or pediatric patients as required. External fixation systems consist of various components that are used to build fixator assemblies unique to the patient's needs. These devices are modular therefore, a multitude of different fixator frame configurations are possible. External fixation devices are used for the following indications:

    1. Fractures and disease which generally may result in joint contractures or loss of range of motion and fractures requiring distraction
    2. Open and closed fracture fixation
    3. Pseudoarthrosis of long bones
    4. Limb lengthening by distraction (not applicable for use with COMPASS Universal Hinge)
    5. Correction of bony or soft tissue deformities (not applicable for use with COMPASS Universal Hinge).
    6. Joint arthrodesis (not applicable for use with COMPASS Universal Hinge)
    7. Infected fractures
    8. Nonunions

    The indications for use listed above cover many of the external fixation systems marketed by Smith & Nephew. These indications are similar to the indications of the predicate devices. The device is intended for single use.

    Device Description

    The subject of this Traditional 510k is the Circular Fixation with Balanced Cable Transport. Originally, the subject device was identified as the ILIZAROV with Balanced Cable Transport. It has since been decided as a company's decision to change the name of the subject device to Circular Fixation with Balanced Cable Transport. In addition, there was an update to the indications for use language since the Pre-Submission. The subject Circular Fixation with Balanced Cable Transport is a product line addition to the predicate, ILIZAROV Pulley System. The Circular Fixation with Balanced Cable Transport consists of cables, pulleys, and the new subject devices, the struts. The existing cables and pulleys are cleared on a similar external fixation system, the predicate ILIZAROV Pulley System, via premarket notification K042436 S.E. 10/07/2004. In the subject, Circular Fixation with Balanced Cable Transport, the cable is routed through the bone segment and exits through soft tissue. Cables are available in diameter of 1.8mm and a length of 1200mm. The subject telescopic rod or a modified strut acting as a motor is attached to the ring-based circular fixation construct. The subject device is turned to pull the cable and move the bone segments in order to perform bone transport and limb lengthening. The advantages of using the subject Circular Fixation with Balanced Cable Transport, include the ability to use fewer half pins and wires. Fewer half pins and wires will create less soft tissue disruption, eliminating the need to pull pins and wires through the skin and soft tissue as the bone moves.

    AI/ML Overview

    The provided document is a 510(k) summary for a medical device called "Circular Fixation with Balanced Cable Transport." This document focuses on demonstrating substantial equivalence to a predicate device based on material, intended use, and performance characteristics through bench testing. It does not describe a clinical study involving AI assistance, multi-reader multi-case studies, or the establishment of ground truth by expert consensus or pathology for an image-based diagnostic device.

    Therefore, the requested information regarding acceptance criteria and performance for an AI-based device, including sample sizes, expert involvement, and clinical study methodologies, cannot be extracted from this document. The document pertains to a mechanical orthopedic device.

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