# Neuropro Spinaljaxx, Inc.

- Location (FDA's records): Modesto, CA
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: MAX (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 0 (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
- Globus Medical, Inc.: 3 (https://510kreport.com/company/globus-medical)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)
- Nanovis, LLC: 1 (https://510kreport.com/company/nanovis)

## Recent decisions
- K152501: Spinal Jaxx Interbody Fusion Device (Jun 29, 2016)

Source page: https://510kreport.com/company/neuropro-spinaljaxx