K251900 is an FDA 510(k) clearance for the MY01 Continuous Compartmental Pressure Monitor. This device is classified as a Monitor, Pressure, Intracompartmental.
Submitted by MY01, Inc. (Montreal, CA). The FDA issued a Cleared decision on January 16, 2026, 210 days after receiving the submission on June 20, 2025.
This device falls under the Orthopedic FDA review panel.
| 510(k) Number | K251900 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 20, 2025 |
| Decision Date | January 16, 2026 |
| Days to Decision | 210 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | LXC - Monitor, Pressure, Intracompartmental |
| Device Class | - |