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510(k) Data Aggregation

    K Number
    K021556
    Manufacturer
    Date Cleared
    2002-08-09

    (88 days)

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

    SYNTHES 2.4 MM CANNULATED COMPRESSION SCREW

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

    Synthes 2.4 mm Cannulated Compression Screw is intended for fixation of fractures and non-unions of small bones and small bone arthrodeses, including, but not limited to, scaphoid fractures; intra-articular fractures of the tarsals, metatarsals, carpals and metacarpals; bunionectomies and osteotomies; arthrodeses of small joints (e.g. phalanges); fractures of the patella, ulna and radial styloid.

    Device Description

    Synthes 2.4 mm Cannulated Compression Screw is a partially threaded self-tapping and self-drilling screw that can be guided into a position using a guidewire. The threaded head is designed to be recessed below or sit flush with the near cortex and features a StarDrive™ head. Synthes 2.4 mm Cannulated Compression Screws are available in various lengths.

    AI/ML Overview

    This document describes a medical device, the Synthes 2.4 mm Cannulated Compression Screw, and its substantial equivalence to a predicate device. It does not contain information on acceptance criteria, device performance, sample sizes for test or training sets, expert qualifications, ground truth establishment, or any studies (MRMC or standalone AI performance).

    Therefore, I cannot provide the requested information. The provided text is a 510(k) summary and FDA clearance letter, which outlines the device's classification, predicate device, intended use, and materials but does not include clinical study data or performance metrics in the format requested for AI/software-based devices.

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