# Spine Next America

- Location (FDA's records): Queenstown, MD
- FDA decisions: 5 (2004–2004): 5 510(k) clearances
- Names in FDA's records: Spine Next America (3); Spine Next America Corporation (2)
- Product codes: MNI (2), MQP (2), KWQ (1)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 3 (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
- Depuyacromed: 3 (https://510kreport.com/company/depuyacromed)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Medtronic Sofamor Danek: 2 (https://510kreport.com/company/medtronic-sofamor-danek)
- Ebi, L.P.: 1 (https://510kreport.com/company/ebi)

## Firms that cite its devices most
- Blackstone Medical, Inc.: 1 (https://510kreport.com/company/blackstone-medical)
- Corentec Co., Ltd.: 1 (https://510kreport.com/company/corentec)
- Sintea Plustek, LLC: 1 (https://510kreport.com/company/sintea-plustek)

## Its most-cited devices
- K042714: Fidji-Vertebral Body Replacement Type 1, 2, 3 and 4 (2004), cited by 3

## Recent decisions
- K042713: Fidji-Vertebral Body Replacement Type 5 (Dec 29, 2004)
- K042714: Fidji-Vertebral Body Replacement Type 1, 2, 3 and 4 (Dec 29, 2004)
- K033965: Shiraz-Anterior System (Mar 4, 2004)
- K033947: Shiraz Posterior System (Mar 4, 2004)
- K033772: Shiraz-Java Spinal Fixation System (Jan 27, 2004)

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