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The UNIPLATE Anterior Cervical Plate System is intended for anterior cervical intervertebral body fixation. This system is indicated for patients in which stability is desired following anterior cervical fusion for the indications listed below. The intended levels for treatment range from C2-T1.

Indications include symptomatic cervical spondylosis, trauma, fracture, posttraumatic kyphosis or lordosis, turnor, degenerative disc disease (defined as discogenic pain with degeneration of the disc confirmed by history and radiographic studies), spinal stenosis, re-operation for failed fusion, or instability following surgery for the above indications.

The UNIPLATE Anterior Cervical Plate System consists of an assortment of plates and screws. The UNIPLATE Anterior Cervical Plate System also contains Class I manual surgical instruments and cases that are considered exempt from premarket notification. Manufactured from ASTM F 136 implant grade titanium Materials: alloy.

The provided text describes a 510(k) submission for a medical device and does not contain information about a study proving the device meets acceptance criteria or details about AI/algorithm performance. It is a regulatory submission for a spinal implant, which typically relies on mechanical testing and comparison to predicate devices, rather than AI performance studies or human reader studies.

Therefore, I cannot fulfill the request as it asks for information not present in the provided context. The document focuses on regulatory approval based on substantial equivalence and mechanical performance data, not a study evaluating algorithm performance or human reader improvement with AI.

To directly answer the prompt based on the absence of information:

1. Table of acceptance criteria and reported device performance: Not applicable. The document refers to "Performance data per ASTM F 1717" being submitted to characterize the device but does not provide specific acceptance criteria or detailed results of those tests.
2. Sample size used for the test set and the data provenance: Not applicable. This document is for a spinal implant, not an AI/algorithm-based device. "Test set" in this context would refer to mechanical testing of the implant, not a data set for an algorithm. Data provenance is not mentioned.
3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts: Not applicable. Ground truth as typically defined for AI/algorithm studies (e.g., expert consensus on medical images) is not relevant to the regulatory submission for this physical medical device.
4. Adjudication method: Not applicable.
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: No, an MRMC study was not done, as this is a physical medical device (spinal plate) and not an AI or imaging diagnosis device.
6. If a standalone (i.e. algorithm only without human-in-the loop performance) was done: No, a standalone algorithm performance study was not done, as this is a physical medical device.
7. The type of ground truth used: Not applicable in the context of AI/algorithm ground truth. The "ground truth" for this device would be its mechanical properties, established through standardized ASTM testing.
8. The sample size for the training set: Not applicable, as this is not an AI/algorithm device.
9. How the ground truth for the training set was established: Not applicable, as this is not an AI/algorithm device.

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The C-Tek® MaxAnTM Anterior Cervical Plate System is intended for anterior interbody fixation of the cervical spine. Indications for use include the temporary stabilization of the anterior spine during the development of cervical fusions in patients with degenerative disc disease (as defined by neck pain of discogenic origin confirmed by patient history and radiographic studies), trauma including fractures, tumors, deformity (defined as kyphosis, lordosis, or scoliosis), pseudarthroses, and/or failed previous fusions. The intended levels for treatment range from C2 - T1.

The C-Tek® MaxAn™ Anterior Cervical Plate System consists of titanium alloy plates and screws. Screws are provided in both fixed and variable versions in sizes 4.0 mm and 4.5 mm with lengths from 8-26 mm. Screws will be provided in both sterile and nonsterile configurations. Cervical plates are provided in both sterile and non-sterile configurations for 1 - 6 levels and in appropriate lengths from 8-150 mm.

The provided text describes a 510(k) premarket notification for a medical device called the C-Tek® MaxAn™ Anterior Cervical Plate System. This is a spinal intervertebral body fixation orthosis.

Based on the document, this is not an AI/ML medical device. It is a traditional medical device (a physical implantable system of plates and screws). Therefore, many of the requested fields related to AI/ML device studies (such as sample size for training/test sets, expert adjudication, MRMC studies, standalone performance, etc.) are not applicable and cannot be extracted from this type of submission.

Here's a breakdown of the information that is available and a note on what is not applicable:

Acceptance Criteria and Reported Device Performance

Study Details:

1. Sample size used for the test set and the data provenance: Not applicable for this type of medical device (physical implant). The "test set" would refer to the physical prototypes tested in non-clinical lab settings. The document does not specify the number of samples or prototypes tested. Data provenance is not relevant in the context of clinical data for an AI/ML device.
2. Number of experts used to establish the ground truth for the test set and the qualifications of those experts: Not applicable. Ground truth, in the context of an AI/ML device, refers to verified labels for data. For a physical medical device, "ground truth" would relate to engineering specifications and performance standards.
3. Adjudication method (e.g. 2+1, 3+1, none) for the test set: Not applicable. This refers to methods for consensus building among human experts labeling data, which is not relevant for this device.
4. 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: Not applicable. This is not an AI/ML device and human readers are not involved in its "performance" in this context.
5. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done: Not applicable. This is not an AI/ML device.
6. The type of ground truth used (expert consensus, pathology, outcomes data, etc.): For this physical device, the "ground truth" for performance is likely based on engineering specifications, material properties (ASTM F-136 for Ti-6Al-4V), and biomechanical testing standards for spinal implants, demonstrating equivalency to predicate devices. The document explicitly states "Non-clinical laboratory testing was performed to determine substantial equivalence."
7. The sample size for the training set: Not applicable. This is not an AI/ML device.
8. How the ground truth for the training set was established: Not applicable. This is not an AI/ML device.

Additional Information from the Submission:

• Device Description: The C-Tek® MaxAn™ Anterior Cervical Plate System consists of titanium alloy plates and screws. Screws are provided in both fixed and variable versions in sizes 4.0 mm and 4.5 mm with lengths from 8-26 mm, in both sterile and non-sterile configurations. Cervical plates are provided in both sterile and non-sterile configurations for 1-6 levels and in lengths from 8-150 mm.
• Materials: Titanium alloy (Ti-6Al-4V, ASTM F-136).
• Predicate Device(s):
  • EBI Anterior Cervical Plate System (Cyprus Anterior Cervical Plating System), K060379
  • EAGLE+ Anterior Cervical Plate system, K070994, K040197
  • Swift Plus Anterior Cervical Plate System, K072546, K040655
• Performance Claim: "The technological characteristics of the C-Tek® MaxAn™ Anterior Cervical Plate System are the same as, or similar to, the predicate devices."
• Study Conclusion: "Non-clinical laboratory testing was performed to determine substantial equivalence. The results indicated that the devices are functional within the intended use."

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