# Footbridge Medical

- Location (FDA's records): Charlotte, NC
- FDA decisions: 1 (2024–2024): 1 510(k) clearance
- Product codes: HRS (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)

## Firms that cite its devices most
- Hyperflex Medical: 1 (https://510kreport.com/company/hyperflex-medical)

## Its most-cited devices
- K241995: HyperFlex™ Bunion Correction System (2024), cited by 1

## Recent decisions
- K241995: HyperFlex™ Bunion Correction System (Nov 26, 2024)

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