Cleared Traditional

K833006 - CEPHALOMETER & FIXATOR

K833006 is an FDA 510(k) clearance for CEPHALOMETER & FIXATOR, manufactured by Modern Systems, Inc.. The device is a Class 2 Radiology device with product code EAG cleared through the Traditional 510(k) pathway after a 119-day FDA review.

K833006 · Modern Systems, Inc. · Radiology device
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Jan 1984
Decision
119d
Days
Class 2
Risk

K833006 is an FDA 510(k) clearance for the CEPHALOMETER & FIXATOR. Classified as Cephalometer (product code EAG), Class II - Special Controls.

Submitted by Modern Systems, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 3, 1984 after a review of 119 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1830 - the FDA radiology and imaging software oversight 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 Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Modern Systems, Inc. devices

FDA 510(k) Submission Details - K833006

510(k) Number K833006 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 06, 1983
Decision Date January 03, 1984
Days to Decision 119 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
12d slower than avg
Panel avg: 107d · This submission: 119d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EAG Device Classification - Class 2, Special Controls

Product Code EAG Cephalometer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1830
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.