# K221410: Maestro Platform

- Pathway: 510(k) (Traditional)
- Applicant: Moon Surgical
- Decided: Dec 2, 2022 after 200 days
- Product code: FQO (Table, Operating-Room, Ac-Powered)
- Device class: 1
- Regulation: 21 CFR 878.4960
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K936308 (1994). 1 ancestor in all.
3 later devices descend from it; 2 cite 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)
- K936308: Endex Endoscopic Positioning System, Andronic Devices, Ltd. (1994) Summary page 4.

## Most influential descendants
- K240598: Maestro System (REF100) (2024), 2 descendants of its own
- K242323: Maestro System (REF100) (2025), 1 descendant of its own
- K250984: Maestro System (REF100) (2025), 0 descendants of its own

## Indications for use
The Maestro System is intended to hold and position laparoscopes and laparoscopic instruments during laparoscopic surgical procedures.

Source page: https://510kreport.com/device/K221410
Methodology: https://510kreport.com/methodology