# K051133: Arcadis Avantic

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Jun 1, 2005 after 29 days
- Product code: OXO (Image-Intensified Fluoroscopic X-Ray System, Mobile)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K912470 (1991). 16 ancestors in all.
20 later devices descend from it; 3 cite it directly.
0 of 37 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040066: Siremobile C06, Siemens Medical Solutions USA, Inc. (2004) Summary page 1.
- K040675: Axiom Artis U, Siemens Medical Systems, Inc. (2004) Summary page 1.

## Most influential descendants
- K132094: Cios Alpha (2014), 19 descendants of its own
- K153244: Cios Fusion (2016), 15 descendants of its own
- K181550: Cios Spin (2018), 10 descendants of its own
- K181560: Cios Alpha (2018), 10 descendants of its own
- K203504: Cios Flow (2020), 9 descendants of its own

## Indications for use
The ARCADIS Avantic is a mobile x-ray system which can operate in six different modes: Digital Radiography, Fluoroscopy, Pulsed Fluoroscopy, Digital Cine Mode (DCM), Subtraction, and Roadmapping, which are necessary to perform a wide variety of clinical procedures. Clinical applications may include, but are not limited to, card/vascular, gastroenterology, electrophysiology, urologic, orthopedic, neurologic, pediatrics, endoscopy, pain therapy and emergency room procedures

Source page: https://510kreport.com/device/K051133
Methodology: https://510kreport.com/methodology