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For photocoagulation during ophthalmic surgery. This device delivers laser energy to target tissue, causing coagulation. Spot size can be varied by altering the distance between the tissue and the probe tip.

The Innovatech Straight Laser Probe is an ophthalmic laser delivery device. By its design, it does not generate, intensify or significantly reduce energy. It consists of a connector that is plugged into an existing laser source, a glass fiber with PVC jacket, a Delrin handpiece and a 304 stainless needle. The specific laser source to which the probe is connected will be specified in the "Indications for Use."

The Innovatech Straight Laser Probe is an ophthalmic laser delivery device, and its acceptance criteria and the study proving it meets these criteria are outlined in the provided text, primarily through a substantial equivalence comparison to predicate devices.

1. Table of Acceptance Criteria and Reported Device Performance

The acceptance criteria for the Innovatech Straight Laser Probe are implicitly defined by its substantial equivalence to predicate devices, meaning its performance characteristics are comparable to those already legally marketed. The table below summarizes the key features and their performance (or characteristics) for the Innovatech device and its primary predicate, the Peregrine Straight Laser Probe (Product: PD600.00, 510(k): K024061).

2. Sample Size Used for the Test Set and Data Provenance

The provided text does not contain information about a specific "test set" in the context of clinical or performance testing with human subjects or a defined dataset for AI evaluation. The substantial equivalence claim is based on a comparison of device specifications and intended use against existing predicate devices. Therefore, there is no information on sample size or data provenance (country of origin, retrospective/prospective).

3. Number of Experts Used to Establish Ground Truth for the Test Set and Qualifications

Since there is no mention of a "test set" in the context of clinical performance or AI evaluation, there is no information provided on the number of experts or their qualifications used to establish ground truth.

4. Adjudication Method for the Test Set

As there is no described test set involving expert review, there is no adjudication method mentioned.

5. If a Multi Reader Multi Case (MRMC) Comparative Effectiveness Study Was Done

No MRMC comparative effectiveness study is mentioned. The submission focuses on device characteristics and substantial equivalence, not comparative effectiveness with or without AI assistance.

6. If a Standalone (Algorithm Only Without Human-in-the-Loop Performance) Was Done

The device is a physical ophthalmic laser probe, not an artificial intelligence algorithm. Therefore, no standalone (algorithm only) performance study was conducted or is relevant.

7. The Type of Ground Truth Used

The "ground truth" for this device's acceptance is based on engineering specifications and functional characteristics being substantially equivalent to legally marketed predicate devices. This is a technical and regulatory comparison, not a clinical "ground truth" derived from expert consensus, pathology, or outcomes data in the typical sense of diagnostic or treatment efficacy studies.

8. The Sample Size for the Training Set

Since this is a physical medical device and not an AI algorithm, there is no concept of a "training set" as understood in machine learning.

9. How the Ground Truth for the Training Set Was Established

As there is no training set, this question is not applicable.

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For photocoagulation during ophthalmic surgery. To be used with (specified equipment).
For photocoagulation during ophthalmic surgery. This device delivers laser energy to target tissue, causing coagulation. Spot size can be varied by altering the distance between the tissue and the probe tip.

The Peregrine Straight Laser Probe is an ophthalmic laser delivery device. By its design, it does not generate, intensify or significantly reduce energy. It consists of a connector that is plugged into an existing laser source, a glass fiber with PVC jacket, a Delrin handpiece and 304 stainless needle. The specific laser source to which the probe is connected will be specified in the "Indications for Use."

The provided text is a 510(k) Premarket Notification summary for the Peregrine Straight Laser Probe. It describes the device, its intended use, and its substantial equivalence to predicate devices, focusing on manufacturing and materials rather than performance data from a clinical study. Therefore, the document does not contain the information required to populate the acceptance criteria and study details as requested. This type of submission typically focuses on demonstrating equivalence to an already approved device through design, materials, and intended use, rather than presenting novel performance data from human or extensive animal studies.

Specifically, the document does not include:

1. A table of acceptance criteria and reported device performance.
2. Details on sample sizes, data provenance, or the nature of any test sets.
3. Information about experts, ground truth establishment, or adjudication methods for performance evaluation.
4. Any mention of a multi-reader multi-case (MRMC) comparative effectiveness study or related effect sizes.
5. Standalone (algorithm-only) performance data.
6. Details on the type of ground truth used for performance evaluation, beyond inferring that the probe is intended to achieve photocoagulation.
7. Information on training set sample sizes or how their ground truth was established, as this is not an AI/ML device submission.

The closest relevant information is about sterility, where it states:

• Acceptance Criteria (Implied): The device will be ETO Sterilized to achieve sterility.
• Study (Method): The method used to validate the sterilization cycle is the AAMI Overkill Method. This is a standard validation method for sterilization, but no specific performance data (e.g., sterility assurance level achieved) is reported in this summary.

In summary, the provided text describes a medical device in the context of a 510(k) submission, which focuses on device description, indications for use, and substantial equivalence to predicate devices. It does not contain the detailed performance study data requested in your prompt.

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