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510(k) Data Aggregation

    K Number
    K954385
    Manufacturer
    Date Cleared
    1996-03-08

    (171 days)

    Product Code
    Regulation Number
    872.4760
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    SYNTHES MANDIBULAR MODULAR FIXATION SYSTEM

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

    Oral, maxillofacial surgery: trauma; surgical correction of dentofacial deformities; . reconstructive surgery; and craniofacial surgery
    ENT: trauma of the nasal bones .
    Neurosurgery: osteosynthesis of the cranial bones. .

    Device Description

    The Synthes Mandibular Modular Fixation System is a plate and screw system, manufactured from commercially pure titanium, and is intended for use in:

    • Oral, maxillofacial surgery: trauma; surgical correction of dentofacial deformities; . reconstructive surgery; and craniofacial surgery
    • ENT: trauma of the nasal bones .
    • Neurosurgery: osteosynthesis of the cranial bones. .
      The plates are available in a variety of shapes and sizes and attach to bone via 2.0 mm, 2.4 mm, or 2.7 mm self-tapping screws.
      Synthes will provide the device non-sterile. Of course, non-sterile devices must be sterilized prior to use; moist heat sterilization is recommended.
    AI/ML Overview

    This document is a 510(k) Summary for a medical device called the "Synthes Mandibular Modular Fixation System." It focuses on demonstrating substantial equivalence to a predicate device through mechanical testing. It does not present information related to acceptance criteria or studies involving device performance in the context of AI, human readers, ground truth, or statistical sample sizes in a clinical or imaging diagnostic setting.

    Therefore, I cannot provide the requested information regarding acceptance criteria, device performance, AI study details, or ground truth establishment based on the provided text. The document describes a traditional medical device (plate and screw system) and its mechanical testing for regulatory clearance, not a diagnostic AI or imaging device study.

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