K220952 is an FDA 510(k) clearance for the MY01 Continuous Compartmental Pressure Monitor. Classified as Monitor, Pressure, Intracompartmental (product code LXC).
Submitted by MY01, Inc. (Montreal, CA). The FDA issued a Cleared decision on May 24, 2022 after a review of 53 days - a notably fast clearance cycle.
This device falls under the Orthopedic FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.
Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.
View all MY01, Inc. devices