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510(k) Data Aggregation

    K Number
    K153180
    Manufacturer
    Date Cleared
    2015-11-25

    (22 days)

    Product Code
    Regulation Number
    888.3040
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    Tyber Medical MST Trauma Screw

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

    The Tyber Medical MST Trauma Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation of bones appropriate for the size of the device. Screws are intended for single use only.

    Device Description

    General trauma screw for compression and fixation of bone with modified surface treatment (MST). The screws will be provided sterile in both solid and cannulated form, made of from titanium.

    AI/ML Overview

    The provided text describes the regulatory clearance of a medical device (Tyber Medical MST Trauma Screw) and includes a summary of nonclinical testing. However, it does not contain information relevant to AI/ML device performance, such as acceptance criteria for algorithms, sample sizes for AI training/test sets, expert adjudication methods, or MRMC studies.

    Therefore, I cannot provide a response that includes items 1-9 as requested, as these pertain specifically to AI/ML device evaluations which are not present in this document.

    The document primarily focuses on demonstrating substantial equivalence to a predicate device through nonclinical testing, materials, and indications for use.

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