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The Modified Shoulder Fixation System is intended for fractures and fracture dislocations, osteotomies, and non-unions of the proximal Humerus.

The Modified Shoulder Fixation System is a set of orthopedic plates and fasteners supplied in a sterilization tray together with several reusable and disposable tools. The set of orthopedic plates and fasteners provided in the sterilization tray consists of the following implantable devices: Shoulder Plates Shoulder Nail Plates Multidirectional and 90° Lock Screws 90° Set Screws Pegs Included in the sterilization tray are the following re-useable instruments: Peg drivers Other standard surgical tools.

The provided text does not contain information about the acceptance criteria or a study proving that the device meets those criteria.

The document is a 510(k) premarket notification summary for a medical device called the "Modified Shoulder Fixation System." It details administrative information such as the device name, predicate device, classification, indications for use, and a general description of the system. It also includes a letter from the FDA confirming substantial equivalence to a predicate device.

Specifically, the document does not include:

1. A table of acceptance criteria or reported device performance.
2. Details about sample sizes, data provenance, or study design for testing.
3. Information on experts, ground truth establishment, or adjudication methods.
4. Any mention of multi-reader multi-case (MRMC) comparative effectiveness studies or standalone algorithm performance.
5. Information about training sets or how ground truth for training was established.

Instead, the summary states: "The Modified Shoulder Fixation System is substantially equivalent to the predicate Shoulder Fixation System. The equivalence was confirmed through pre-clinical testing." This implies that the basis for approval was a demonstration of substantial equivalence to an already legally marketed device, often involving comparison of design, materials, and potentially certain mechanical tests, rather than clinical performance studies against specific acceptance criteria.

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The Modified Shoulder Fixation System is intended for fractures and fracture dislocations, osteotomies, and non-unions of the proximal Humerus.

The Modified Shoulder Fixation System is a set of orthopedic plates and fasteners supplied in a sterilization tray together with several reusable and disposable tools. The set of orthopedic plates and fasteners provided in the sterilization tray consists of the following implantable devices: • Shoulder Plates • Multidirectional and 90° Lock Screws • 90° Set Screws • Pegs Also, provided in the sterilization tray are the re-useable instruments

1. Table of Acceptance Criteria and Reported Device Performance:

The provided document does not contain explicit acceptance criteria and device performance metrics in the format of a table. Instead, it describes a "Summary of Substantial Equivalence" and states that "The equivalence was confirmed through pre-clinical testing."

2. Sample size used for the test set and the data provenance:

The document does not specify a distinct "test set" or its sample size. The substantial equivalence was confirmed through "pre-clinical testing," which typically involves mechanical and/or bench testing rather than studies with patient data. Therefore, data provenance in terms of country of origin or retrospective/prospective is not applicable as patient data was not used.

3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts:

This information is not provided in the document. Given that the equivalence was based on "pre-clinical testing," ground truth would likely be established through engineering specifications and test standards, not expert medical consensus on a test set.

4. Adjudication method (e.g. 2+1, 3+1, none) for the test set:

This information is not provided. As mentioned, the evaluation was based on pre-clinical testing, making formal adjudication methods for a medical test set irrelevant.

5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance:

A multi-reader multi-case (MRMC) comparative effectiveness study was not done. The device is a physical orthopedic implant (Shoulder Fixation System) and not an AI-powered diagnostic or assistive tool for human readers. Therefore, there is no discussion of human reader improvement with or without AI assistance.

6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done:

A "standalone" performance study in the context of an algorithm or AI was not done. The device is a physical orthopedic implant, not an algorithm.

7. The type of ground truth used (expert consensus, pathology, outcomes data, etc.):

The ground truth for demonstrating substantial equivalence was based on pre-clinical testing which would involve engineering and mechanical performance data, often compared against established standards for material properties and mechanical strength of similar devices. It is not based on expert consensus, pathology, or outcomes data in the clinical sense.

8. The sample size for the training set:

The concept of a "training set" is not applicable as this is a medical device (implant) clearance, not an AI or machine learning model.

9. How the ground truth for the training set was established:

Not applicable, as there is no training set for this type of device.

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Ask a specific question about this device