# Rubicon Spine, LLC

- Location (FDA's records): Sarasota, FL
- FDA decisions: 1 (2018–2018): 1 510(k) clearance
- Product codes: MAX (1)
- Predicates its devices cite: 8 (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
- Synthes Spine: 2 (https://510kreport.com/company/synthes-spine)
- Stryker Corp.: 2 (https://510kreport.com/company/stryker)
- Integrity Spine Lumbar Interbody Fusion System: 1 (https://510kreport.com/company/integrity-spine-lumbar-interbody-fusion-system)
- Vertebron, Inc.: 1 (https://510kreport.com/company/vertebron)
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)
- Infront Medical, LLC: 1 (https://510kreport.com/company/infront-medical)

## Recent decisions
- K181030: Rubicon Lumbar Interbody Fusion System (Jul 17, 2018)

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