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510(k) Data Aggregation

    K Number
    K222097
    Manufacturer
    Date Cleared
    2023-05-04

    (290 days)

    Product Code
    Regulation Number
    888.3010
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    OLYMPIC Deformity Band System

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

    The OLYMPIC Deformity Band System is a temporary implant for use in orthopedic surgery. The band system is intended to provide temporary stabilization as a bone anchor during the development of solid bony fusion and aid in the repair of bone fractures. The indications for use include the following applications:
    -Spinal trauma surgery, used in sublaminar or facet wiring techniques.
    -Spinal reconstructive surgery, incorporated into constructs for the purpose of correction of spinal deformities such as idiopathic and neuromuscular scoliosis in patients 8 years of age or older, adult scoliosis, kyphosis and spondylolisthesis. -Spinal degenerative surgery, as an adjunct to spinal fusions.
    The OLYMPIC Deformity Band System may also be used in conjunction with other medical grade implants made of similar metals whenever "wiring" may help secure the attachment of the other implants.

    Device Description

    The OLYMPIC Deformity Band System is a system designed to stabilize a vertebrae during the fusion process. The system is composed of sublaminar bad cerclages and band connectors. The system is supported by a comprehensive set of instruments to install the implants within the system. All implant components are manufactured from the materials listed in the table below.

    AI/ML Overview

    This is a medical device, not an AI/ML device. The provided text outlines the 510(k) summary for the OLYMPIC Deformity Band System, a temporary orthopedic implant, and its substantial equivalence to predicate devices, but it does not contain information about acceptance criteria or a study proving device performance in the context of an AI/ML model.

    Therefore, I cannot provide the requested information. The document focuses on mechanical and material testing for a physical implant, not on the performance metrics of an AI system.

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