# K240926: PeekMed web

- Pathway: 510(k) (Traditional)
- Applicant: Peek Health, S.A.
- Decided: Dec 6, 2024 after 246 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K896095 (1990). 23 ancestors in all.
6 later devices descend from it; 2 cite it directly.
0 of 30 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222767: PeekMed web (v1), Peek Health, S.A. (2022) Summary page 4.

## Most influential descendants
- K250042: PeekMed web (2025), 4 descendants of its own
- K251096: PeekMed web (2025), 3 descendants of its own
- K252856: PeekMed web (2025), 1 descendant of its own
- K261641: Lower Limb AI (LLAI) (2026), 0 descendants of its own
- K252452: PeekMed web (2025), 0 descendants of its own

## Indications for use
PeekMed web is a system designed to help healthcare professionals carry out pre-operative planning for several surgical procedures, based on their imported patients’ imaging studies. Experience in usage and a clinical assessment is necessary for the proper use of the system in the revision and approval of the output of the planning. The multi-platform system works with a database of digital representations related to surgical materials supplied by their manufacturers.

Source page: https://510kreport.com/device/K240926
Methodology: https://510kreport.com/methodology