# Summit Spine

- Location (FDA's records): Georgetown, TX
- FDA decisions: 2 (2017–2017): 2 510(k) clearances
- Product codes: MAX (1), ODP (1)
- Predicates its devices cite: 1 (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
- Eminent Spine: 1 (https://510kreport.com/company/eminent-spine)

## Firms that cite its devices most
- Pantheon Spinal: 1 (https://510kreport.com/company/pantheon-spinal)
- Sync Surgical: 1 (https://510kreport.com/company/sync-surgical)

## Its most-cited devices
- K170572: Summit Spine Yellowstone Lumbar Interbody Fusion System (2017), cited by 1
- K163494: Summit Spine Channel Cervical Interbody Fusion System (2017), cited by 1

## Recent decisions
- K163494: Summit Spine Channel Cervical Interbody Fusion System (Jun 20, 2017)
- K170572: Summit Spine Yellowstone Lumbar Interbody Fusion System (Apr 26, 2017)

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