Cleared Traditional

K222818 - Xpedition Powered Stair Chair (62570000...

K222818 is an FDA 510(k) clearance for Xpedition Powered Stair Chair (62570000..., manufactured by Stryker Medical. The device is a Class 2 Physical Medicine device with product code ILK cleared through the Traditional 510(k) pathway after a 127-day FDA review.

K222818 · Stryker Medical · Physical Medicine device
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Jan 2023
Decision
127d
Days
Class 2
Risk

K222818 is an FDA 510(k) clearance for the Xpedition ™ Powered Stair Chair (625700000000). Classified as Transport, Patient, Powered (product code ILK), Class II - Special Controls.

Submitted by Stryker Medical (Portage, US). The FDA issued a Cleared decision on January 24, 2023 after a review of 127 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5150 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

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FDA 510(k) Submission Details - K222818

510(k) Number K222818 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 19, 2022
Decision Date January 24, 2023
Days to Decision 127 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
12d slower than avg
Panel avg: 115d · This submission: 127d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ILK Device Classification - Class 2, Special Controls

Product Code ILK Transport, Patient, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5150
Definition A Powered Patient Transport Is A Motorized Device Intended For Use In Mitigating Mobility Impairment Caused By Injury Or Other Disease By Moving A Person From One Location Or Level To Another, Such As Up And Down Flights Of Stairs (e.g., Attendant-operated Portable Stair-climbing Chairs). This Generic Type Of Device Does Not Include Motorized Three-wheeled Vehicles Or Wheelchairs.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Physical Medicine devices follow this clearance model.