# Spinal Kinetics / Orthofix / Seaspine

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 1 (2024–2024): 1 510(k) clearance
- Product codes: QLQ (1)
- Predicates its devices cite: 1 (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
- Spinal Kinetics, LLC: 1 (https://510kreport.com/company/spinal-kinetics)

## Recent decisions
- K241117: M6-C™ Single Use, Disposable Instrumentation (Jun 21, 2024)

Source page: https://510kreport.com/company/spinal-kinetics-orthofix-seaspine