FDA 510(k) Applications Submitted by Ryan Matthew
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K243950 | 12/23/2024 | ARVIS« Shoulder | Kico Knee Innovation Company Pty Ltd |
| K243980 | 12/23/2024 | ARVIS Surgical Navigation System | Kico Knee Innovation Company Pty Limited |
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