# Arthro-Dif

- Location (FDA's records): Fr. Myers, FL
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: NKB (1)
- Predicates its devices cite: 4 (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
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)
- Aesculap Implant Systems, LLC: 1 (https://510kreport.com/company/aesculap-implant-systems)
- Ldr Spine USA: 1 (https://510kreport.com/company/ldr-spine-usa)
- GS Medical Co., Ltd.: 1 (https://510kreport.com/company/gs-medical)

## Recent decisions
- K141695: Acrosspine Pedicle Screw System (Dec 30, 2014)

Source page: https://510kreport.com/company/arthro-dif