K874502 is an FDA 510(k) clearance for the GAIT-AID ORTHOPEDIC INSOLE. Classified as Orthosis, Limb Brace (product code IQI), Class I - General Controls.
Submitted by Gait-Aid, Inc. (Ontario, Canada, CA). The FDA issued a Cleared decision on November 30, 1987 after a review of 28 days - a notably fast clearance cycle.
This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3475 - the FDA physical medicine device framework. 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 Gait-Aid, Inc. devices