Cleared Special

K071949 - VICTORY

K071949 is an FDA 510(k) clearance for VICTORY, manufactured by Pride Mobility Products Corp.. The device is a Class 2 Physical Medicine device with product code INI cleared through the Special 510(k) pathway after a 19-day FDA review.

K071949 · Pride Mobility Products Corp. · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2007
Decision
19d
Days
Class 2
Risk

K071949 is an FDA 510(k) clearance for the VICTORY, 4 WHEEL SCOOTER / MODEL, # SC1740. Classified as Vehicle, Motorized 3-wheeled (product code INI), Class II - Special Controls.

Submitted by Pride Mobility Products Corp. (Exeter, US). The FDA issued a Cleared decision on August 1, 2007 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3800 - the FDA physical medicine device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Pride Mobility Products Corp. devices

FDA 510(k) Submission Details - K071949

510(k) Number K071949 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 2007
Decision Date August 01, 2007
Days to Decision 19 days
Submission Type Special
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
96d faster than avg
Panel avg: 115d · This submission: 19d
Pathway characteristics
Modification to existing cleared device.

INI Device Classification - Class 2, Special Controls

Product Code INI Vehicle, Motorized 3-wheeled
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.3800
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 - INI Vehicle, Motorized 3-wheeled

All 128
Devices cleared under the same product code (INI) and FDA review panel - the closest regulatory comparables to K071949.
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K063389 · Pride Mobility Products Corp. · Nov 2006