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510(k) Data Aggregation

    K Number
    K052505
    Date Cleared
    2005-11-04

    (52 days)

    Product Code
    Regulation Number
    874.3620
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    CALF IMPLANT, MODEL EC17-X

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

    The Caff Implants (Silicone Carving Blocks) are for augmentation and reconstructive surgery. The Implantech Calf Implants are carvable to allow the surgeon to shape the device should additional shaping be desired.

    Device Description

    Calf Implant (Silicone Carving Blocks)

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for a Gluteal Implant (later identified as a Calf Implant in the "Indications for Use" section). It confirms substantial equivalence to a predicate device.

    However, the document does not contain any information about acceptance criteria or the study that proves the device meets those criteria. The 510(k) clearance process primarily focuses on demonstrating substantial equivalence to a legally marketed predicate device, not necessarily on presenting detailed performance study data against specific acceptance criteria in the format requested.

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

    To answer your request, I would need a different type of document, such as a summary of safety and effectiveness data (which may be part of a 510(k) submission but is not included in this clearance letter), a clinical study report, or a detailed device specification.

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