# Spine Next SA

- Location (FDA's records): Queenstown, MD
- FDA decisions: 3 (2003–2003): 3 510(k) clearances
- Product codes: JDK (2), MNH (1)
- Predicates its devices cite: 2 (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
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- Depuyacromed: 1 (https://510kreport.com/company/depuyacromed)

## Firms that cite its devices most
- Interbody Innovations, Llp: 1 (https://510kreport.com/company/interbody-innovations)

## Its most-cited devices
- K030871: Fidji Large Cement Restrictor (2003), cited by 1

## Recent decisions
- K030767: Fidji Small Cement Restrictor (Dec 22, 2003)
- K030871: Fidji Large Cement Restrictor (Dec 22, 2003)
- K031265: Shiraz-Java Spinal Fixation System (Oct 9, 2003)

Source page: https://510kreport.com/company/spine-next