# Legend Spine Technologies

- Location (FDA's records): Bethlehem, PA
- FDA decisions: 2 (2018–2019): 2 510(k) clearances
- Product codes: ODP (1), MAX (1)
- Predicates its devices cite: 7 (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
- Medtronic Sofamor Danek USA, Inc.: 2 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Axis Orthopaedics: 1 (https://510kreport.com/company/axis-orthopaedics)
- Zimmer Trabecular Metal Technology: 1 (https://510kreport.com/company/zimmer-trabecular-metal-technology)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- K2m, Inc.: 1 (https://510kreport.com/company/k2m)
- Camber Spine Technologies: 1 (https://510kreport.com/company/camber-spine-technologies)

## Recent decisions
- K192208: CORNICE Cervical Spacer System (Oct 9, 2019)
- K180071: STYLO Interbody Fusion Device (May 3, 2018)

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