Cleared Traditional

K920860 - CONTROLLED PASSIVE MOTION MACHINE

K920860 is the FDA 510(k) clearance for CONTROLLED PASSIVE MOTION MACHINE by U.S. Mfg. & Management, Inc.. It is a Class 1 Physical Medicine device (product code BXB) cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K920860 · U.S. Mfg. & Management, Inc. · Physical Medicine device
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Apr 1992
Decision
37d
Days
Class 1
Risk

K920860 is an FDA 510(k) clearance for the CONTROLLED PASSIVE MOTION MACHINE. Classified as Exerciser, Powered (product code BXB), Class I - General Controls.

Submitted by U.S. Mfg. & Management, Inc. (Bristol, US). The FDA issued a Cleared decision on April 2, 1992 after a review of 37 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5380 - 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 U.S. Mfg. & Management, Inc. devices

Submission Details

510(k) Number K920860 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 25, 1992
Decision Date April 02, 1992
Days to Decision 37 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
78d faster than avg
Panel avg: 115d · This submission: 37d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code BXB Exerciser, Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5380
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 - BXB Exerciser, Powered

All 31
Devices cleared under the same product code (BXB) and FDA review panel - the closest regulatory comparables to K920860.
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