Cleared Traditional

K992354 - SNT IMAGE ANALYSIS SYSTEM

K992354 is the FDA 510(k) clearance for SNT IMAGE ANALYSIS SYSTEM by Surgical Navigation Technologies, Inc.. It is a Class 2 Radiology device (product code LLZ) cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K992354 · Surgical Navigation Technologies, Inc. · Radiology device
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Oct 1999
Decision
90d
Days
Class 2
Risk

K992354 is an FDA 510(k) clearance for the SNT IMAGE ANALYSIS SYSTEM. Classified as System, Image Processing, Radiological within the LLZ classification (a category encompassing advanced image processing and PACS-adjacent software), Class II - Special Controls.

Submitted by Surgical Navigation Technologies, Inc. (Broomfield, US). The FDA issued a Cleared decision on October 12, 1999 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2050 - 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: Incremental AI imaging tool. Moderate equivalence dependency. Overall, this clearance reflects a predicate-aligned approval typical of modern AI radiology extensions - not a novel clinical breakthrough, but a validated iteration within an established regulatory category.

View all Surgical Navigation Technologies, Inc. devices

Submission Details

510(k) Number K992354 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 14, 1999
Decision Date October 12, 1999
Days to Decision 90 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
17d faster than avg
Panel avg: 107d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LLZ System, Image Processing, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2050
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.

Regulatory Peers - LLZ System, Image Processing, Radiological

All 1150
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K992354.
PHILIPS INTURIS DICOM RECORDER
K993227 · Philips Medical Systems North America, Inc. · Dec 1999
AX WORKSTATION DR-VIEWER SOFTWARE OPTION
K992925 · Siemens Corp. · Nov 1999
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K992886 · Toshiba America Medical Systems, In.C · Nov 1999
AX WORKSTATION
K992073 · Siemens Medical Solutions USA, Inc. · Sep 1999
GE VIEW APPLICATIONS (CONSISTING OF GE VIEWING STATION AND GE EXTENDED VIEWING STATION) VERSION 1.2C
K991629 · Ge Medical Systems, Inc. · Aug 1999
IMMERGE IMAGE CORRELATION
K991468 · Surgical Navigation Technologies, Inc. · Jul 1999