Cleared Traditional

K002580 - PRAIRIE CRUISER

K002580 is an FDA 510(k) clearance for PRAIRIE CRUISER, manufactured by Raye'S, Inc.. The device is a Class 2 Physical Medicine device with product code ITI cleared through the Traditional 510(k) pathway after a 319-day FDA review.

K002580 · Raye'S, Inc. · Physical Medicine device
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Jul 2001
Decision
319d
Days
Class 2
Risk

K002580 is an FDA 510(k) clearance for the PRAIRIE CRUISER. Classified as Wheelchair, Powered (product code ITI), Class II - Special Controls.

Submitted by Raye'S, Inc. (Ellis, US). The FDA issued a Cleared decision on July 3, 2001 after a review of 319 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3860 - 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. Elevated predicate reliance profile. 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.

View all Raye'S, Inc. devices

FDA 510(k) Submission Details - K002580

510(k) Number K002580 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 18, 2000
Decision Date July 03, 2001
Days to Decision 319 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
204d slower than avg
Panel avg: 115d · This submission: 319d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ITI Device Classification - Class 2, Special Controls

Product Code ITI Wheelchair, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.3860
Definition A Powered Wheelchair Is A Battery-operated Device With Wheels That Is Intended For Medical Purposes To Provide Mobility To Persons Restricted To A Sitting Position. Fda Interprets “mobility To Persons Restricted To A Sitting Position” To Mean The Device Type Is Intended To Provide Mobility To Individuals Who Have Mobility Impairments And Require An Assistive Device For Mobility. Note: This Type Of Device Is Not Intended To Climb Stairs (see Product Code: Imk).
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.

Regulatory Peers - ITI Wheelchair, Powered

All 353
Devices cleared under the same product code (ITI) and FDA review panel - the closest regulatory comparables to K002580.
XTERRA GT POWER WHEELCHAIR
K012909 · Invacare Corp. · Oct 2001
M71 POWER WHEELCHAIR
K012927 · Invacare Corp. · Sep 2001
QUANTUM BLAST
K011993 · Pride Mobility Products Corp. · Jul 2001
POWER TILT AND RECLINE SYSTEM
K010917 · Sunrise Medical, Inc. · May 2001
OPTIMA
K011053 · Medical Industries America, Inc. · Apr 2001
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K010364 · Invacare Corp. · Mar 2001