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510(k) Data Aggregation

    K Number
    K980486
    Manufacturer
    Date Cleared
    1998-04-14

    (64 days)

    Product Code
    Regulation Number
    888.3350
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    IMPLEX HEP ACETABULAR REVISION CUP, CEMENTED OR CEMENTLESS MODEL A-240 SYSTEM

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

    Intended for use in the acetabulum where severe degeneration, trauma, or other pathology of the hip joint indicates cemented, cementless, or hybrid total hip arthroplasty.

    Device Description

    Implex HEP Acetabular Revision Cups, Cemented or Cementless, are available in OD sizes from 40 mm to 72 mm (in 2 mm increments), and with 4 possible ID size options (22 mm, 26 mm, 28 mm, and 32 mm). Implex HEP Revision Acetabular Cups are to be implanted using the Implex Acetabular Cup Instrumentation System.

    AI/ML Overview

    This document is a 510(k) summary for the Implex HEP Acetabular Cup Revision System. It describes a medical device clearance process by the FDA, not a study performing device performance evaluation against acceptance criteria. Therefore, the information requested by the user is not found in the input document.

    The provided document is a 510(k) premarket notification for a medical device and does not contain information on acceptance criteria, device performance studies, sample sizes, ground truth establishment, or expert-based evaluations as typically detailed in a clinical or performance study report.

    The 510(k) process is primarily a demonstration of "substantial equivalence" to a predicate device, not a comprehensive efficacy or performance study against specific acceptance criteria in the way a clinical trial or a detailed device verification and validation report would.

    Therefore, I cannot provide the requested information from the given text.

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