Cleared Traditional

SONI-LOK SCOPE STABILIZER (K850122) - FDA 510(k) Clearance

Class I General & Plastic Surgery device.

K850122 · Med Surg Designs, Inc. · General & Plastic Surgery device
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Feb 1985
Decision
38d
Days
Class 1
Risk

K850122 is an FDA 510(k) clearance for the SONI-LOK SCOPE STABILIZER. Classified as Holder, Camera, Surgical (product code FXR), Class I - General Controls.

Submitted by Med Surg Designs, Inc. (Chardon, US). The FDA issued a Cleared decision on February 21, 1985 after a review of 38 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4160 - 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 Med Surg Designs, Inc. devices

Submission Details

510(k) Number K850122 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 14, 1985
Decision Date February 21, 1985
Days to Decision 38 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
77d faster than avg
Panel avg: 115d · This submission: 38d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FXR Holder, Camera, Surgical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4160
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.