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510(k) Data Aggregation

    K Number
    K023725
    Date Cleared
    2003-02-03

    (89 days)

    Product Code
    Regulation Number
    878.4750
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    HEMORRHAGE OCCLUDER PIN (HOP), MODEL 337-247

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

    THE HEMORRHAGE OCCLUDER PIN IS INDICATED TO BE USED TO STOP MASSIVE PRESACRAL HEMORRHAGE DURING SURGERY

    Device Description

    HEMORRHAGE OCCLUDER PIN (HOP) is of 7mm length and 8mm pinhead. It is made out of medical grade Titanium suitable for implantation.

    AI/ML Overview

    The provided text is a 510(k) summary for the HEMORRHAGE OCCLUDER PIN (HOP), which is an implantable staple. It primarily focuses on demonstrating substantial equivalence to a predicate device rather than presenting a performance study with acceptance criteria.

    Therefore, the requested information regarding acceptance criteria, device performance, study details (sample size, data provenance, expert adjudication, MRMC, standalone performance, ground truth), and training set details cannot be extracted from this document as such a study is not described.

    The summary states:

    • "This device is safe and effective as the other predicate device cited above. This is better expressed in the tabulated comparison (Paragraph 14 below)"
    • "Please find below a tabulated comparison supporting that this device is substantially equivalent to other medical devices in commercial distribution."

    This indicates that the submission relies on demonstrating similarity to a previously approved device rather than presenting a new clinical performance study with specific acceptance criteria and detailed results.

    In summary, the document does not contain the information required to populate the outlined sections.

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