Cleared Traditional

K831135 - SAUNDERS #7080 CERVICAL TRACTION SYS

K831135 is an FDA 510(k) clearance for SAUNDERS #7080 CERVICAL TRACTION SYS, manufactured by Chattanooga Group, Inc.. The device is a Class 1 Physical Medicine device with product code ILZ cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K831135 · Chattanooga Group, Inc. · Physical Medicine device
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Jun 1983
Decision
78d
Days
Class 1
Risk

K831135 is an FDA 510(k) clearance for the SAUNDERS #7080 CERVICAL TRACTION SYS. Classified as Accessories, Traction (product code ILZ), Class I - General Controls.

Submitted by Chattanooga Group, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 24, 1983 after a review of 78 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5925 - 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 Chattanooga Group, Inc. devices

FDA 510(k) Submission Details - K831135

510(k) Number K831135 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 1983
Decision Date June 24, 1983
Days to Decision 78 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
37d faster than avg
Panel avg: 115d · This submission: 78d
Pathway characteristics
Predicate-based equivalence.

ILZ Device Classification - Class 1, General Controls

Product Code ILZ Accessories, Traction
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5925
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.