Cleared Abbreviated

K071390 - WHEELCHAIR MODEL STS

K071390 is an FDA 510(k) clearance for WHEELCHAIR MODEL STS, manufactured by Innovative Products, Inc.. The device is a Class 2 Physical Medicine device with product code IPL cleared through the Abbreviated 510(k) pathway after a 63-day FDA review.

K071390 · Innovative Products, Inc. · Physical Medicine device
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Jul 2007
Decision
63d
Days
Class 2
Risk

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

FDA 510(k) Submission Details - K071390

510(k) Number K071390 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 18, 2007
Decision Date July 20, 2007
Days to Decision 63 days
Submission Type Abbreviated
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
52d faster than avg
Panel avg: 115d · This submission: 63d
Pathway characteristics
Standards-based clearance path.

IPL Device Classification - Class 2, Special Controls

Product Code IPL Wheelchair, Standup
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.3900
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 - IPL Wheelchair, Standup

All 35
Devices cleared under the same product code (IPL) and FDA review panel - the closest regulatory comparables to K071390.
LEVO C3
K083017 · Levo AG · Oct 2008
BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION)
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LLOYD LINDEN, MODEL E04
K071761 · Lloyd Linden, Inc. · Aug 2007
LSC, MODEL 3
K061726 · Lifestand · Dec 2006
PARAGOLFER
K060936 · Parabasetec, GmbH · Aug 2006
ALILIFE STAND UP POWERED WHEELCHAIR, HC-300
K052375 · Alilife Technological Co., Ltd. · Sep 2005