K071390 is an FDA 510(k) clearance for the WHEELCHAIR MODEL STS. Classified as Wheelchair, Standup (product code IPL), Class II - Special Controls.
Submitted by Innovative Products, Inc. (Grand Forks, US). The FDA issued a Cleared decision on July 20, 2007 after a review of 63 days - a notably fast clearance cycle.
This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3900 - the FDA physical medicine device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.
Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.
View all Innovative Products, Inc. devices