Gait-Aid Orthopedic Insole

FDA 510(k) K874502 · Gait-Aid, Inc.

Substantially Equivalent

510(k) numberK874502

Submission

Device name
Gait-Aid Orthopedic Insole
Applicant
Gait-Aid, Inc.
Ontario, Canada, CA
Received
November 2, 1987
Decision date
November 30, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
IQI – Orthosis, Limb Brace
Device class
Class I (low risk)
Regulation
21 CFR 890.3475
Specialty
Physical Medicine

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K052771Sensor WalkIQI · Traditional Otto Bock Healthcare LP05/03/2006SE
K031576Spartan Orthopaedic Wrist Brace, Model SCT-1IQI · Traditional Surgitech, Inc.07/31/2003SE
K926391Accuflex Dynamic Elbow OrthosisIQI · Traditional Regulatory & Marketing Services, Inc.07/22/1993SE
K910974Mcconnell Shoulder BraceIQI · Traditional Mcconnell Orthopedic03/21/1991SE
K831542Adjustable Polycentric Elbow HingeIQI · Traditional Fred Sammons, Inc.06/24/1983SE
K831615Drop Foot BraceIQI · Traditional Edward Dilauro, Jr.06/15/1983SE
K823812Various Supports and SplintsIQI · Traditional Danek Medical, Inc.01/14/1983SE
K823113Brace-Up All Purpose Wrist BandIQI · Traditional Arco Matic, Inc.11/16/1982SE
K823160Rotation BootIQI · Traditional Warm & Form, Orthopedic Materials11/10/1982SE

Questions and answers

When was Gait-Aid Orthopedic Insole cleared by the FDA?

Gait-Aid Orthopedic Insole (K874502) received a 510(k) decision of Substantially Equivalent on November 30, 1987, 28 days after the submission was received.

What is the product code of K874502?

The FDA product code is IQI – Orthosis, Limb Brace, a Class I (low risk) device regulated under 21 CFR 890.3475.