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510(k) Data Aggregation

    K Number
    K171590
    Date Cleared
    2017-06-27

    (27 days)

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

    The Skeletal Dynamics Distal Elbow Plating System is intended for fixation of fractures, fusions, osteotomies and non-unions of the radius and ulna, particularly in osteopenic bone.

    Device Description

    The Skeletal Dynamics Distal Elbow Plating System is comprised of:

    • Titanium alloy plates and screws in various configurations
    • Cobalt chrome polyaxial screws
    • Stainless steel K-wires (for provisional fixation not for implantation)
    • System specific instrumentation

    The current Skeletal Dynamics Distal Elbow Plating System (K140892) includes the radial head and proximal ulna plates. Plates in double hockey stick, Y and coronoid shape configurations with the same node and inter-node features as the radial head plate are being added for use in the proximal radius and ulna in this submission. All plates are made of medical grade titanium alloy. The radial head, proximal ulna and coronoid plates are offered in left and right applications, the proximal ulna plate is provided in various lengths, and the double hockey stick and Y plates are in single size and have bilateral application. Additional screws length as well as new threaded pegs, washers, polyaxial locking screws, and instruments have been added in the subject system in this submission. The system is provided non-sterile and is sterilized in the user facility.

    AI/ML Overview

    This document is a 510(k) premarket notification for a medical device called the "Skeletal Dynamics Distal Elbow Plating System." It is not about an AI/ML medical device. Therefore, the information requested about acceptance criteria and study design for an AI/ML device, such as sample sizes for test and training sets, number and qualifications of experts, adjudication methods, MRMC studies, standalone AI performance, and ground truth establishment, cannot be found in this document.

    The document describes a traditional orthopaedic medical device (bone plates and screws) and demonstrates its substantial equivalence to previously cleared predicate devices through engineering analysis and preclinical mechanical testing, adhering to ASTM standards. There is no mention of algorithms, artificial intelligence, or machine learning.

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