# K121418: Planmed Verity

- Pathway: 510(k) (Traditional)
- Applicant: Planmed OY
- Decided: Feb 1, 2013 after 266 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: 4 generations back to K973598 (1997). 14 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061834: Xcat; Xcat for Neuro, Xoran Technologies, Inc. (2006) Summary page 2.

## Most influential descendants
- K160723: OnSight 3D Extremity System (2016), 1 descendant of its own
- K252249: Extremity CT Imaging System (2026), 0 descendants of its own

## Indications for use
Planmed Verity is intended to be used for X-ray computed tomography imaging of anatomnies within upper and lower extremities. The device is to be operated and used by legally qualified health care professionals.

Source page: https://510kreport.com/device/K121418
Methodology: https://510kreport.com/methodology