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510(k) Data Aggregation

    K Number
    K993990
    Date Cleared
    2000-02-22

    (90 days)

    Product Code
    Regulation Number
    882.5330
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM

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

    The Leibinger Quik Disk Titanium Clamp System is intended to reattach a cranial bone flap to the surrounding cranium after a craniotomy procedure.

    Device Description

    The Leibinger Quik Disk Titanium Clamp System consists of a two-piece titanium implant and associated nonpowered neurosurgical instruments. The system allows for timely fixation of cranial flaps to the surrounding cranium after craniotomies in lieu of bone plate and screw methods. The Quik Disk has two parallel 15 mm diameter titanium disks that are connected by an internal, serrated breakaway stem and grasping clamp assembly that is fully contained between the two discs.

    AI/ML Overview

    This 510(k) summary describes a medical device, the Leibinger Quik Disk Titanium Clamp System, which is a titanium implant intended for fixing cranial flaps after craniotomies. The provided text does not include any information about acceptance criteria, device performance, or any studies conducted.

    Therefore, I cannot provide the requested information in the table or answer the specific questions about sample size, ground truth, expert qualifications, adjudication methods, or MRMC studies. The document only describes the device, its intended use, and states its substantial equivalence to other legally marketed devices.

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