# Montross Extremity Medical

- Location (FDA's records): Colorado Springs, CO
- FDA decisions: 1 (2023–2023): 1 510(k) clearance
- Product codes: KWD (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ascension Orthopedics, Inc.: 1 (https://510kreport.com/company/ascension-orthopedics)
- Nexa Orthopedics, Inc.: 1 (https://510kreport.com/company/nexa-orthopedics)

## Recent decisions
- K221220: Montross Extremity Medical Hemi Implant System (Apr 19, 2023)

Source page: https://510kreport.com/company/montross-extremity-medical