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510(k) Data Aggregation

    K Number
    K071272
    Date Cleared
    2007-09-12

    (128 days)

    Product Code
    Regulation Number
    884.5300
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K897129

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

    The TROJAN® THINTENSITY™ brand male latex condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted diseases).

    Device Description

    The condoms are made of a natural rubber latex sheath, which completely covers the penis with a closely fitted membrane. The condom is smooth surfaced, straight-walled with a contoured-bulbous section near the closed-end, which terminates with a reservoir tip. The condom has a silicone lubricant. The condom design is within the ASTM standard specifications D-3492, e.q., minimum length 160 mm, maximum width 54 mm, and minimum thickness of 30 uM.

    AI/ML Overview

    The provided text describes a 510(k) summary for a male latex condom, focusing on its substantial equivalence to predicate devices and its intended use. It does not contain information about specific acceptance criteria or a study proving the device meets those criteria in the format requested.

    Therefore, I cannot extract the following information from the provided text:

    1. A table of acceptance criteria and the reported device performance.
    2. Sample size used for the test set and the data provenance.
    3. Number of experts used to establish the ground truth for the test set and their qualifications.
    4. Adjudication method for the test set.
    5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done and its effect size.
    6. If a standalone performance study was done.
    7. The type of ground truth used.
    8. The sample size for the training set.
    9. How the ground truth for the training set was established.

    The document primarily focuses on the administrative aspects of the 510(k) submission, device description, intended use, and technological characteristics, stating conformance with ASTM standard specifications D-3492 as the basis for substantial equivalence. It does not detail the specific test results or study methodologies that would lead to a "reported device performance."

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