Cleared Traditional

K070563 - VIDAR VISION 2000

K070563 is an FDA 510(k) clearance for VIDAR VISION 2000, manufactured by Vidar Systems Corp.. The device is a Class 2 Radiology device with product code MQB cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K070563 · Vidar Systems Corp. · Radiology device
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Mar 2007
Decision
17d
Days
Class 2
Risk

K070563 is an FDA 510(k) clearance for the VIDAR VISION 2000. Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by Vidar Systems Corp. (Waterbury, US). The FDA issued a Cleared decision on March 16, 2007 after a review of 17 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

FDA 510(k) Submission Details - K070563

510(k) Number K070563 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 27, 2007
Decision Date March 16, 2007
Days to Decision 17 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
90d faster than avg
Panel avg: 107d · This submission: 17d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

MQB Device Classification - Class 2, Special Controls

Product Code MQB Solid State X-ray Imager (flat Panel/digital Imager)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1680
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

Bsi Healthcare
JOHN HOWLETT

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 - MQB Solid State X-ray Imager (flat Panel/digital Imager)

All 423
Devices cleared under the same product code (MQB) and FDA review panel - the closest regulatory comparables to K070563.
VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS
K071193 · Vidar Systems Corp. · May 2007
SYNEPIX 4600 DETECTOR
K070829 · Analogic Corporation · May 2007
AGFA COMPUTED RADIOGRAPHY SYSTEM WITH NX2.X WORKSTATIONS
K071162 · Agfa Healthcare Corp. · May 2007
PHILIPS ESSENTA DR
K070528 · Philips Medical Systems GmbH, Dmc · Mar 2007
X3C DIGITAL RADIOGRAPHIC DETECTOR
K070079 · Imaging Dynamics Company , Ltd. · Jan 2007
DX-SI
K063421 · Agfa Corp. · Nov 2006
K070563 · VIDAR VISION 2000
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