Cleared Traditional

K791057 - CAST BRACE COMPONENTS

K791057 is the FDA 510(k) clearance for CAST BRACE COMPONENTS by 3M Company. It is a Class 1 Physical Medicine device (product code IQI) cleared through the Traditional 510(k) pathway after a 12-day FDA review.

K791057 · 3M Company · Physical Medicine device
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Jun 1979
Decision
12d
Days
Class 1
Risk

K791057 is an FDA 510(k) clearance for the CAST BRACE COMPONENTS. Classified as Orthosis, Limb Brace (product code IQI), Class I - General Controls.

Submitted by 3M Company (White City, US). The FDA issued a Cleared decision on June 20, 1979 after a review of 12 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 3M Company devices

Submission Details

510(k) Number K791057 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 08, 1979
Decision Date June 20, 1979
Days to Decision 12 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
103d faster than avg
Panel avg: 115d · This submission: 12d
Pathway characteristics
Predicate-based equivalence.

Device Classification

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 18
Devices cleared under the same product code (IQI) and FDA review panel - the closest regulatory comparables to K791057.
SECUTEX WRIST BRACE
K791249 · Conphar, Inc. · Jul 1979
SECUTEX KNEE BAND
K791266 · Conphar, Inc. · Jul 1979
SECUTEX ANKLE BAND
K791267 · Conphar, Inc. · Jul 1979
FOOT POSITIONER
K781206 · Fred Sammons, Inc. · Jul 1978
ORTHOSISES DEVICES
K780225 · Biomet, Inc. · Feb 1978
BRACE, TENNIS ELBOW
K780053 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jan 1978