# K200756: Kubtec Mozart Supra

- Pathway: 510(k) (Traditional)
- Applicant: Kub Technologies, Inc.
- Decided: Jun 12, 2020 after 80 days
- Product code: MWP (Cabinet, X-Ray System)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K021113 (2002). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071233: Xpert 40 Specimen Radiography System, Kub Technologies, Inc. (2007) Summary page 10.
- K183624: Kubtec Mozart (Xpert42), Kub Technologies, Inc. (2019) Summary page 10.

## Most influential descendants
- K210955: Kubtec Mozart Supra (XPERT 84) Radiography System (2021), 0 descendants of its own

## Indications for use
The MOZART SUPRA Specimen Tomosynthesis System is a Cabinet x-ray system that is specifically designed to provide high detail radiographic imaging of surgically excised medical specimens from various anatomical regions, i.e. breast, both in 2-dimensional and 3-dimensional tomosynthesis views.

Source page: https://510kreport.com/device/K200756
Methodology: https://510kreport.com/methodology