# K221929: Smith+Nephew INTELLIO Tablet

- Pathway: 510(k) (Traditional)
- Applicant: Smith+Nephew
- Decided: Sep 6, 2022 after 67 days
- Product code: ODA (Endoscopic Central Control Unit)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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 K833587 (1983). 39 ancestors in all.
No later device cites it as a predicate yet.
0 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K203566: Tablet Application, Smith & Nephew (2021) Summary page 4.

## Indications for use
The Smith+Nephew INTELLIO Tablet is indicated for use to provide wired or wireless remote control of Smith+Nephew compatible surgical and endoscopic devices within the operating room including camera/camera control unit, patient information system, mechanical resection system, fluid management system and RF coblation system. These controls consist of adjusting parameter settings only.

Source page: https://510kreport.com/device/K221929
Methodology: https://510kreport.com/methodology