Cleared Traditional

K951771 - COMMUNITY BALANCE PERFORMANCE MONITOR OR COMMUNITY BPM

K951771 is an FDA 510(k) clearance for COMMUNITY BALANCE PERFORMANCE MONITOR O..., manufactured by Sms Technologies, Ltd.. The device is a Class 1 Physical Medicine device with product code KHX cleared through the Traditional 510(k) pathway after a 116-day FDA review.

K951771 · Sms Technologies, Ltd. · Physical Medicine device
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Aug 1995
Decision
116d
Days
Class 1
Risk

K951771 is an FDA 510(k) clearance for the COMMUNITY BALANCE PERFORMANCE MONITOR OR COMMUNITY BPM. Classified as Platform, Force-measuring (product code KHX), Class I - General Controls.

Submitted by Sms Technologies, Ltd. (Harlow, Essex, GB). The FDA issued a Cleared decision on August 11, 1995 after a review of 116 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.1575 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Sms Technologies, Ltd. devices

FDA 510(k) Submission Details - K951771

510(k) Number K951771 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 17, 1995
Decision Date August 11, 1995
Days to Decision 116 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
1d slower than avg
Panel avg: 115d · This submission: 116d
Pathway characteristics
Predicate-based equivalence.

KHX Device Classification - Class 1, General Controls

Product Code KHX Platform, Force-measuring
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.1575
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.