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510(k) Data Aggregation

    K Number
    K981372
    Manufacturer
    Date Cleared
    1998-05-11

    (25 days)

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

    SYNTHES 3.0 MM PC-FIX SYSTEM

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

    The Synthes 3.0 mm PC-Fix™ is a long bone and small bone plate and screw system, intended to treat fractures of various bones, including the radius, ulna, distal tibia, pelvis, clavicle, fibula, humerus, and scapula.

    Device Description

    The Synthes 3.0 mm PC-FixTM is a plate and screw system. The plate shares normal weight-bearing forces/load with the fixed fractured bone. and is fixed to the bone with locking screws, bridging the fracture as it heals. The plate neutralizes most of the torsional, shear and bending forces that would otherwise be transferred to the fracture site. This system is designed to be less invasive, as stripping of the periosteum is not recommended; reduce the risk of infection, refracture, implant failure, and loss of reduction (and subsequent complications); allow for early weight-bearing and carly implant removal; and reduce surgery time (no screw measuring, simpler procedure). The plates are available as Straight. T-shaped, and Reconstruction in commercially pure titanium. The screws are available in titanium alloy.

    AI/ML Overview

    This document is a 510(k) summary for the Synthes 3.0 mm PC-Fix™ System, a bone plate and bone screw system. It declares that the device is substantially equivalent to a predicate device and is approved for marketing.

    It does not contain information about acceptance criteria or a study that proves the device meets acceptance criteria.

    The document details:

    • Device Description: The Synthes 3.0 mm PC-Fix™ is a plate and screw system designed to share normal weight-bearing forces with fractured bone, fixed with locking screws to bridge the fracture as it heals. It neutralizes torsional, shear, and bending forces. It's designed to be less invasive, reduce infection risk, allow early weight-bearing and implant removal, and reduce surgery time. The plates are available in Straight, T-shaped, and Reconstruction designs in commercially pure titanium; screws are titanium alloy.
    • Intended Use: To treat fractures of various bones, including the radius, ulna, distal tibia, pelvis, clavicle, fibula, humerus, and scapula.
    • Materials: Plates from commercially pure titanium, screws from titanium alloy.
    • Predicate Device: Synthes PC-Fix.
    • Regulatory Classification: Class II, 21 CFR 888.3030 and 888.3040.
    • Warnings and Restrictions: The device is not approved for pedicular screw attachment or fixation to the posterior elements of the cervical, thoracic, or lumbar spine. If used for such purposes, it's considered investigational.

    Therefore, I cannot extract the requested information regarding acceptance criteria and a study proving their fulfillment from the provided text.

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