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510(k) Data Aggregation

    K Number
    K183581
    Date Cleared
    2019-01-20

    (30 days)

    Product Code
    Regulation Number
    882.4305
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    Codman Disposable Perforators

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

    The Codman Disposable Perforator is for use in perforating the cranium. When properly used, it is designed to automatically disengage once perforation is accomplished and when pressure is removed from the drill point.

    Device Description

    The Codman Disposable Perforators are pre-assembled, single-use, sterile devices that are designed to perforate the cranium. When properly used, the Disposable Perforators are designed to automatically disengage once perforation is accomplished and when pressure is removed from the drill point. They are designed with a Hudson end and are available in three color-coded sizes:

    • 14mm (blue ABS sleeve) – product number: 26-1221
    • 11mm (green ABS sleeve) product number: 26-1222 ●
    • 9mm (yellow ABS sleeve) product number: 26-1223 ●
    AI/ML Overview

    This document describes a 510(k) premarket notification for "Codman Disposable Perforators," which are medical devices used to perforate the cranium. The submission aims to demonstrate substantial equivalence to previously cleared devices.

    Here's an analysis of the acceptance criteria and study that proves the device meets them:

    1. A table of acceptance criteria and the reported device performance

    TestTest Method / PurposeAcceptance CriteriaResult
    Full Dose Mapping ValidationEstablish a new gamma radiation sterilization cycle in compliance with ISO 11137-1Dose Uniformity Ratio:
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