Cleared Special

K051315 - MODIFICATION TO: SECTRA IDS5 WORKSTATION

K051315 is an FDA 510(k) clearance for MODIFICATION TO: SECTRA IDS5 WORKSTATION, manufactured by Sectra-Imtec AB. The device is a Class 2 Radiology device with product code LLZ cleared through the Special 510(k) pathway after a 26-day FDA review.

K051315 · Sectra-Imtec AB · Radiology device
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Jun 2005
Decision
26d
Days
Class 2
Risk

K051315 is an FDA 510(k) clearance for the MODIFICATION TO: SECTRA IDS5 WORKSTATION. 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 Sectra-Imtec AB (Denton, US). The FDA issued a Cleared decision on June 15, 2005 after a review of 26 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Incremental AI imaging tool. Low regulatory complexity profile. 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 Sectra-Imtec AB devices

FDA 510(k) Submission Details - K051315

510(k) Number K051315 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 20, 2005
Decision Date June 15, 2005
Days to Decision 26 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
81d faster than avg
Panel avg: 107d · This submission: 26d
Pathway characteristics
Modification to existing cleared device.

LLZ Device Classification - Class 2, Special Controls

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 1307
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K051315.
FUJI SYNAPSE WORKSTATION SOFTWARE
K051553 · Fujifilm Medical Systems U.S.A, Inc. · Jul 2005
REGIUS RS-1000, MEDICAL IMAGE PROCESSING WORKSTATION
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E1 MEDICAL FLAT PANEL DISPLAY SYSTEM AND MFGD 1218 MEDICAL FLAT PANEL DISPLAY
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GE VIEWPOINT
K050943 · General Electric Co. · May 2005
20.8-INCH (53CM) COLOR LCD MONITOR, MODELS CDL2112A, CCL350I & DV3MC-HB
K050619 · Totoku Electric Co., Ltd. · Apr 2005