Cleared Traditional

ORTHOTIC LEG GAIT CORRECTOR DEVICE (K800716) - FDA 510(k) Clearance

Class I Physical Medicine device.

K800716 · Ipos Luneburg · Physical Medicine device
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May 1980
Decision
32d
Days
Class 1
Risk

K800716 is an FDA 510(k) clearance for the ORTHOTIC LEG GAIT CORRECTOR DEVICE. Classified as Twister, Brace Setting (product code ITO), Class I - General Controls.

Submitted by Ipos Luneburg (Mchenry, US). The FDA issued a Cleared decision on May 2, 1980 after a review of 32 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3410 - 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 Ipos Luneburg devices

Submission Details

510(k) Number K800716 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 31, 1980
Decision Date May 02, 1980
Days to Decision 32 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
83d faster than avg
Panel avg: 115d · This submission: 32d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code ITO Twister, Brace Setting
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3410
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.