# K071233: Xpert 40 Specimen Radiography System

- Pathway: 510(k) (Traditional)
- Applicant: Kub Technologies, Inc.
- Decided: Jun 20, 2007 after 48 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: 2 generations back to K021113 (2002). 4 ancestors in all.
18 later devices descend from it; 5 cite it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052433: Pixarray 100 Digital Specimen Radiography (DSR) System, Bioptics, Inc. (2005) Summary page 2.
- K061361: Faxitron Digital Radiography System, Model DX-50, Faxitron X-Ray Corp. (2006) Summary page 2.
- K953404: Osteo-Ray 100, Micro Focus Imaging, Inc. (1995) Summary page 2.

## Most influential descendants
- K083510: Kubtec Xpert 20 (2009), 15 descendants of its own
- K111508: Trident Specimen Radiography System, Model : RC Tri-00001 (2011), 14 descendants of its own
- K122428: Faxitron Specien Radiography System (2012), 4 descendants of its own
- K183624: Kubtec Mozart (Xpert42) (2019), 3 descendants of its own
- K182727: Trident HD Specimen Radiography System (2019), 3 descendants of its own

## Indications for use
Provide digital x-ray images of harvested tissue specimens from various anatomical regions in order to provide rapid verification that the correct tissue has been excised during the biopsy procedure.

Source page: https://510kreport.com/device/K071233
Methodology: https://510kreport.com/methodology