# Amplitude

- Location (FDA's records): Valence, FR
- FDA decisions: 2 (2017–2023): 2 510(k) clearances
- Product codes: JWH (2)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 1 (1 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
- Howmedica Osteonics Corp.: 3 (https://510kreport.com/company/howmedica-osteonics)
- Zimmer, Inc.: 2 (https://510kreport.com/company/zimmer)
- Maxx Orthopedics, Inc.: 2 (https://510kreport.com/company/maxx-orthopedics)

## Its most-cited devices
- K161414: Anatomic Total Knee System (2017), cited by 1

## Recent decisions
- K230078: TRAX® CR Total Knee System (Nov 3, 2023)
- K161414: Anatomic Total Knee System (Jan 19, 2017)

Source page: https://510kreport.com/company/amplitude