# K203216: The Multimodality Advanced Vessel Analysis

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems Nederland B.V.
- Decided: Nov 25, 2020 after 23 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K971684 (1997). 123 ancestors in all.
1 later device descends from it; 1 cites it directly.
3 of 125 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060937: Brilliance Volume, Philips Medical Systems (Cleveland), Inc. (2006) Summary page 6.
- K112020: Syngo.CT Vascular Analysis, Siemens Medi Cal Solutions, Inc. (2011) Summary page 6.
- K130749: Syngo.MR General; Syngo.MR Cardiology; Syngo.MR Vascular, Siemens Medical Solutions USA, Inc. (2013) Summary page 6.

## Most influential descendants
- K253735: AV Vascular (2026), 0 descendants of its own

## Indications for use
The Multimodality Advanced Vessels Analysis (MM AVA) application is intended for visualization, assessment and quantification of vascular datasets.

Source page: https://510kreport.com/device/K203216
Methodology: https://510kreport.com/methodology