Cleared Traditional

PHYSIOTRON(TM) MICROSURGICAL MOTOR & COOLING SYS. (K882654) - FDA 510(k) Clearance

Class I General & Plastic Surgery device.

K882654 · Surgical Innovators of America, Inc. · General & Plastic Surgery device
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Sep 1988
Decision
83d
Days
Class 1
Risk

K882654 is an FDA 510(k) clearance for the PHYSIOTRON(TM) MICROSURGICAL MOTOR & COOLING SYS.. Classified as Motor, Surgical Instrument, Ac-powered (product code GEY), Class I - General Controls.

Submitted by Surgical Innovators of America, Inc. (New York, US). The FDA issued a Cleared decision on September 20, 1988 after a review of 83 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4820 - the FDA general and plastic surgery 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 Surgical Innovators of America, Inc. devices

Submission Details

510(k) Number K882654 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 29, 1988
Decision Date September 20, 1988
Days to Decision 83 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
32d faster than avg
Panel avg: 115d · This submission: 83d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GEY Motor, Surgical Instrument, Ac-powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4820
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.