Cleared Traditional

K874502 - GAIT-AID ORTHOPEDIC INSOLE

K874502 is an FDA 510(k) clearance for GAIT-AID ORTHOPEDIC INSOLE, manufactured by Gait-Aid, Inc.. The device is a Class 1 Physical Medicine device with product code IQI cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K874502 · Gait-Aid, Inc. · Physical Medicine device
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Nov 1987
Decision
28d
Days
Class 1
Risk

K874502 is an FDA 510(k) clearance for the GAIT-AID ORTHOPEDIC INSOLE. Classified as Orthosis, Limb Brace (product code IQI), Class I - General Controls.

Submitted by Gait-Aid, Inc. (Ontario, Canada, CA). The FDA issued a Cleared decision on November 30, 1987 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3475 - 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 Gait-Aid, Inc. devices

FDA 510(k) Submission Details - K874502

510(k) Number K874502 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 02, 1987
Decision Date November 30, 1987
Days to Decision 28 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
87d faster than avg
Panel avg: 115d · This submission: 28d
Pathway characteristics
Predicate-based equivalence.

IQI Device Classification - Class 1, General Controls

Product Code IQI Orthosis, Limb Brace
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3475
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - IQI Orthosis, Limb Brace

All 24
Devices cleared under the same product code (IQI) and FDA review panel - the closest regulatory comparables to K874502.
Neurosplint
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ADJUSTABLE POLYCENTRIC ELBOW HINGE
K831542 · Fred Sammons, Inc. · Jun 1983
VARIOUS SUPPORTS AND SPLINTS
K823812 · Danek Medical, Inc. · Jan 1983
ROTATION BOOT
K823160 · Warm & Form, Orthopedic Materials · Nov 1982