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510(k) Data Aggregation

    K Number
    K992570
    Date Cleared
    1999-09-01

    (30 days)

    Product Code
    Regulation Number
    888.3360
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    UNITRAX C-TAPER NECK ADJUSTMENT SLEEVE

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

    The indications for use of the Unitrax® C-Taper Neck Adjustment Sleeve, in keeping with those of the legally marketed predicate devices, are as follows: For Use as a Hemi-Hip Replacement: - Femoral head/neck fractures or non-unions. - Aseptic necrosis of the femoral head/neck - Osteo- and post traumatic arthritis

    Device Description

    This Special 510(k) submission is intended to address a design modification to the predicate Unitrax® V40™ Neck Adjustment Sleeve. The Unitrax® V40™ Neck Adjustment Sleeve is a tapered sleeve component whose outer diameter mates with the bore of the Unitrax® Unipolar Head, and inner diameter mates with the trunnion neck of the femoral stem. The design modification involves changing the inner taper diameter of the current sleeve component. The modified device will allow Unitrax® Unipolar Heads to be compatible with Osteonics C-Taper femoral stems. The modified component, the Unitrax® C-Taper Neck Adjustment Sleeve, is substantially equivalent to the predicate device which was cleared for marketing via the 510(k) process. The Unitrax® C-Taper Neck Adjustment Sleeves are manufactured from wrought cobaltchromium alloy, which conforms to ASTM F-1537. The intended use of the subject Unitrax® C-Taper Neck Adjustment Sleeve is identical to that of the Unitrax® V40™ Neck Adjustment Sleeve.

    AI/ML Overview

    This is a medical device, not an AI/ML device, therefore, the requested information is not applicable.

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