# Medtronic Midas Rex

- Location (FDA's records): Fort Worth, TX
- FDA decisions: 1 (2002–2002): 1 510(k) clearance
- Product codes: HBB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (0 its own)
- Recalls linked to its devices: 9 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medtronic Powered Surgical Solutions: 5 (https://510kreport.com/company/medtronic-powered-surgical-solutions)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)
- Medicon EG: 1 (https://510kreport.com/company/medicon-eg)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Zethon, Ltd.: 1 (https://510kreport.com/company/zethon)
- Linvatec Corp.: 1 (https://510kreport.com/company/linvatec)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)

## Its most-cited devices
- K020069: Medtronic Mida Rex Legend System, Midas Rex Legend Pneumatic High Speed System or Legend System (2002), cited by 11

## Recent decisions
- K020069: Medtronic Mida Rex Legend System, Midas Rex Legend Pneumatic High Speed System or Legend System (Mar 18, 2002)

Source page: https://510kreport.com/company/medtronic-midas-rex