Cleared Traditional

K010941 - THE NIMBLE ROCKET POWERED WHEELCHAIR

K010941 is an FDA 510(k) clearance for THE NIMBLE ROCKET POWERED WHEELCHAIR, manufactured by Nimble, Inc.. The device is a Class 2 Physical Medicine device with product code ITI cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K010941 · Nimble, Inc. · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2001
Decision
85d
Days
Class 2
Risk

K010941 is an FDA 510(k) clearance for the THE NIMBLE ROCKET POWERED WHEELCHAIR. Classified as Wheelchair, Powered (product code ITI), Class II - Special Controls.

Submitted by Nimble, Inc. (Great Neck, US). The FDA issued a Cleared decision on June 22, 2001 after a review of 85 days - a notably fast clearance cycle.

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: 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 Nimble, Inc. devices

FDA 510(k) Submission Details - K010941

510(k) Number K010941 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 29, 2001
Decision Date June 22, 2001
Days to Decision 85 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
30d faster than avg
Panel avg: 115d · This submission: 85d
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 362
Devices cleared under the same product code (ITI) and FDA review panel - the closest regulatory comparables to K010941.
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
MCC-MIV ONE 2 ONE SOFTWARE
K010364 · Invacare Corp. · Mar 2001