Search Results

The intended use of the device is as a wheelchair. The wheelchair and drive system empower physically challenged persons by providing a means of mobility. This includes temporary and permanent conditions in all ages, including but not limited to Arthritis, paraplegic, Quadriplegic, Multiple Sclerosis and other immobilizing or debilitating conditions. Our device and the predicate device provide the same function for occupants who are unable to move due to injuries or other medical conditions.

The MyCycle Handmaster Victory wheelchair comprises a wheelchair and a drive unit for powering the wheelchair. The wheelchair comprises a substantially identical device as the Quickie 2hp Titanium Wheelchair. The measurements of each dimension, as well as the construction materials, and the type of welding techniques utilized are substantially identical. based on the documentation available to applicant regarding this wheelchair. The only difference is that the MyCvcle device is not of Titanium but of conventional metal materials. However, the maximum weight bearing capacity, the tiltover testing, the dimensions and the weight of the device are identical.

The provided text describes a 510(k) submission for the MyCycle Handmaster Victory Wheelchair. It does not contain information about acceptance criteria or a study proving the device meets specific performance criteria through testing. Instead, the submission relies on demonstrating substantial equivalence to a predicate device.

Here's a breakdown of why the requested information cannot be fully provided:

• Reliance on Predicate Device: The core of this 510(k) is that "Inasmuch as the device is substantially identical in every dimension to the Quickie 2hp Titanium Wheelchair, the same test results that are exhibited by the Quickie 2hp Titanium Wheelchair are applicable to the MyCycle Handmaster Light Wheelchair." This means MyCycle did not conduct independent performance studies to establish acceptance criteria for their device. They are asserting that the predicate device's existing performance data applies.

The following information summarizes what is available in the provided text, addressing the points where possible, and explicitly stating when information is not present.

1. Table of Acceptance Criteria and Reported Device Performance

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

• Sample Size for Test Set: Not applicable. The MyCycle device itself was not independently tested to establish these criteria. The submission relies on the existing performance data of the predicate device (Quickie 2hp Titanium Wheelchair). The sample size for the predicate device's original testing is not provided in this document.
• Data Provenance: Not applicable for MyCycle's device directly. The "documentation available to applicant regarding this wheelchair" for the predicate device is mentioned, but its specific provenance (country, retrospective/prospective) is not detailed.

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

• Not applicable. No independent "ground truth" establishment or expert review for the MyCycle device's performance data is described, as it relies on the predicate device's existing data.

4. Adjudication Method for the Test Set

• Not applicable. No independent testing or adjudication for the MyCycle device's performance is described.

5. Multi Reader Multi Case (MRMC) Comparative Effectiveness Study

• No. This is not applicable to a wheelchair device's performance assessment. MRMC studies are typically for medical imaging diagnostics involving human readers and AI systems.

6. Standalone (Algorithm Only Without Human-in-the-Loop Performance) Study

• No. This is not applicable. The device is a physical wheelchair, not an algorithm or AI system.

7. Type of Ground Truth Used

• Not applicable for the MyCycle device directly. The "ground truth" for the performance claims is implicitly the established and accepted performance of the predicate device (Quickie 2hp Titanium Wheelchair) through its own testing and regulatory clearance.

8. Sample Size for the Training Set

• Not applicable. The device is a physical product, not an AI/ML algorithm that requires a training set.

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

• Not applicable. See point 8.

Ask a specific question about this device