# K130893: Xperct Rel. 3

- Pathway: 510(k) (Abbreviated)
- Applicant: Philips Medical Systems Nederland B.V.
- Decided: Sep 6, 2013 after 158 days
- Product code: OWB (Interventional Fluoroscopic X-Ray System)
- 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: 2 generations back to K042646 (2004). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060749: Xperct, Philips Medical Systems North America Co. (2006) Summary page 1.

## Most influential descendants
- K201583: SmartCT R1.0 (2021), 1 descendant of its own
- K253670: SmartCT (R3.0 (L10)) (2026), 0 descendants of its own

## Indications for use
The XperCT Rel. 3 reconstructs 3D volumes from rotational fluoroscopic acquisitions, and provides CT-like images that assist the physician with diagnosis, surgical planning, interventional procedures, and treatment follow-up. XperCT ReL 3 helps to manually estimate the dimension of the lesion.

Source page: https://510kreport.com/device/K130893
Methodology: https://510kreport.com/methodology