Cleared Abbreviated

K071331 - VITREA VERSION 4.0

K071331 is an FDA 510(k) clearance for VITREA VERSION 4.0, manufactured by Vital Images, Inc.. The device is a Class 2 Radiology device with product code LLZ cleared through the Abbreviated 510(k) pathway after a 14-day FDA review.

K071331 · Vital Images, Inc. · Radiology device
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May 2007
Decision
14d
Days
Class 2
Risk

K071331 is an FDA 510(k) clearance for the VITREA VERSION 4.0. 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 Vital Images, Inc. (Minnetonka, US). The FDA issued a Cleared decision on May 25, 2007 after a review of 14 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 Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Incremental AI imaging tool. Standards-verified equivalence. 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 Vital Images, Inc. devices

FDA 510(k) Submission Details - K071331

510(k) Number K071331 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 11, 2007
Decision Date May 25, 2007
Days to Decision 14 days
Submission Type Abbreviated
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
93d faster than avg
Panel avg: 107d · This submission: 14d
Pathway characteristics
Standards-based clearance path. Third-party reviewed.

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 Consultant

Regulatory Technology Services, LLC
MARK JOB

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - LLZ System, Image Processing, Radiological

All 1724
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K071331.
REGIUS UNITEA
K071436 · Konica Minolta Medical & Graphic, Inc. · Jun 2007
IMAGE-ARENA APPLICATIONS AND RESEARCH-ARENA APPLICATIONS
K071232 · Tomtec Imaging Systems GmbH · Jun 2007
VITAL CONNECT 4.1
K071362 · Vital Images, Inc. · May 2007
SYNGO IMAGING (VERSION V30)
K071114 · Siemens AG Medical Solutions · May 2007
QLAB QUANTIFICATION
K070792 · Philips Ultrasound, Inc. · Apr 2007
NIO 5MP-21 AND MDNG-5121 CB
K062621 · Barcoview · Mar 2007