# Spinenet, LLC

- Location (FDA's records): Winter Park, FL
- FDA decisions: 2 (2011–2020): 2 510(k) clearances
- Product codes: KWQ (1), ODP (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Zavation, LLC: 1 (https://510kreport.com/company/zavation)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Spinal Elements, Inc.: 1 (https://510kreport.com/company/spinal-elements)
- Sulzer Spine-Tech: 1 (https://510kreport.com/company/sulzer-spine-tech)
- Calvary Spine, LLC: 1 (https://510kreport.com/company/calvary-spine)

## Firms that cite its devices most
- Spinefrontier, Inc.: 2 (https://510kreport.com/company/spinefrontier)
- Integrity Spine: 1 (https://510kreport.com/company/integrity-spine)
- Maxim Surgical: 1 (https://510kreport.com/company/maxim-surgical)
- Kalitec Direct, LLC: 1 (https://510kreport.com/company/kalitec-direct)

## Its most-cited devices
- K110733: Daytona Anterior Cervical Cage (2011), cited by 5

## Recent decisions
- K200170: SpineNet SSP System (Feb 5, 2020)
- K110733: Daytona Anterior Cervical Cage (Aug 25, 2011)

Source page: https://510kreport.com/company/spinenet