Cleared Traditional

K961307 - SMART SPOT

K961307 is the FDA 510(k) clearance for SMART SPOT by Cmt Medical Technologies, Ltd.. It is a Class 2 Radiology device (product code LLZ) cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K961307 · Cmt Medical Technologies, Ltd. · Radiology device
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Jul 1996
Decision
88d
Days
Class 2
Risk

K961307 is an FDA 510(k) clearance for the SMART SPOT. 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 Cmt Medical Technologies, Ltd. (Haifa, IL). The FDA issued a Cleared decision on July 1, 1996 after a review of 88 days - a notably fast clearance cycle.

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 Cmt Medical Technologies, Ltd. devices

Submission Details

510(k) Number K961307 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 04, 1996
Decision Date July 01, 1996
Days to Decision 88 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
19d faster than avg
Panel avg: 107d · This submission: 88d
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 1057
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K961307.
FLOUROSPOT T.O.P.
K961871 · Siemens Medical Solutions USA, Inc. · Jul 1996
ADVANTAGE WINDOWS WITH FUNCTOOL OPTION
K960265 · GE Medical Systems · Jul 1996
PICKER MR WORKSTATIONS (VISTAR,MONTAGE AND ONCALL)
K961637 · Philips Medical Systems (Cleveland), Inc. · Jul 1996
PHILIPS EASYVISION
K953911 · Philips Medical Systems, Inc. · Jun 1996
DIGISCAN 2 PLUS
K955457 · Siemens Medical Solutions USA, Inc. · Jun 1996
GE ADVANTAGE WINDOWS REVIEW WORKSTATION
K960613 · GE Medical Systems · Apr 1996