# K180918: Planmed Verity

- Pathway: 510(k) (Traditional)
- Applicant: Planmed OY
- Decided: Nov 30, 2018 after 235 days
- Product code: OAS (X-Ray, Tomography, Computed, Dental)
- 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: 5 generations back to K973598 (1997). 15 ancestors in all.
1 later device descends 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)
- K143435: Planmed Verity, Planmed OY (2015) Summary page 4.

## Most influential descendants
- K213278: Planmed Verity (2022), 0 descendants of its own

## Indications for use
Planmed Verity is intended to be used for X-ray computed cone beam tomography imaging of anatomies within upper and lower extremities, head and neck.

Source page: https://510kreport.com/device/K180918
Methodology: https://510kreport.com/methodology