Cleared Traditional

K010721 - AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM

K010721 is an FDA 510(k) clearance for AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM, manufactured by Siemens Medical Corp.. The device is a Class 2 Radiology device with product code IZI cleared through the Traditional 510(k) pathway after a 18-day FDA review.

K010721 · Siemens Medical Corp. · Radiology device
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Mar 2001
Decision
18d
Days
Class 2
Risk

K010721 is an FDA 510(k) clearance for the AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM. Classified as System, X-ray, Angiographic (product code IZI), Class II - Special Controls.

Submitted by Siemens Medical Corp. (Iselin, US). The FDA issued a Cleared decision on March 30, 2001 after a review of 18 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1600 - 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.

View all Siemens Medical Corp. devices

FDA 510(k) Submission Details - K010721

510(k) Number K010721 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 12, 2001
Decision Date March 30, 2001
Days to Decision 18 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
89d faster than avg
Panel avg: 107d · This submission: 18d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IZI Device Classification - Class 2, Special Controls

Product Code IZI System, X-ray, Angiographic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1600
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 - IZI System, X-ray, Angiographic

All 102
Devices cleared under the same product code (IZI) and FDA review panel - the closest regulatory comparables to K010721.
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