# Integrity Spine Lumbar Interbody Fusion System

- Location (FDA's records): San Antonio, TX
- FDA decisions: 1 (2015–2015): 1 510(k) clearance
- Product codes: MAX (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (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
- Difusion Technologies: 1 (https://510kreport.com/company/difusion-technologies)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)

## Firms that cite its devices most
- Rubicon Spine, LLC: 1 (https://510kreport.com/company/rubicon-spine)
- Bluestone Synergy: 1 (https://510kreport.com/company/bluestone-synergy)

## Its most-cited devices
- K151819: Integrity Spine Lumbar Interbody Fusion System (2015), cited by 2

## Recent decisions
- K151819: Integrity Spine Lumbar Interbody Fusion System (Nov 10, 2015)

Source page: https://510kreport.com/company/integrity-spine-lumbar-interbody-fusion-system