# Nlt Spine, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 8 (2011–2016): 8 510(k) clearances
- Product codes: MAX (5), HRX (3)
- Predicates its devices cite: 23 (9 its own); citations of its devices by later devices: 12 (9 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
- Globus Medical, Inc.: 3 (https://510kreport.com/company/globus-medical)
- Life Spine, Inc.: 1 (https://510kreport.com/company/life-spine)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Trans1 Incorporated: 1 (https://510kreport.com/company/trans1)
- Custom Spine, Inc.: 1 (https://510kreport.com/company/custom-spine)
- Theken Spine, LLC: 1 (https://510kreport.com/company/theken-spine)

## Firms that cite its devices most
- SeaSpine Orthopedics Corporation: 1 (https://510kreport.com/company/seaspine-orthopedics)
- Nu Vasive, Incorporated: 1 (https://510kreport.com/company/nu-vasive)
- Benvenue Medical, Inc.: 1 (https://510kreport.com/company/benvenue-medical)

## Its most-cited devices
- K112359: Prow Fusion (2011), cited by 3
- K130254: Prow Fusion (2013), cited by 3
- K120553: ESPIN (2012), cited by 2
- K153786: Prow Fusion-V (2016), cited by 2
- K151654: Prow Fusion (2015), cited by 1
- K130057: ESPIN (2013), cited by 1

## Recent decisions
- K153665: Prow Fusion-L (Sep 15, 2016)
- K153786: Prow Fusion-V (Jul 11, 2016)
- K151654: Prow Fusion (Jul 17, 2015)
- K133061: Espin System (Nov 27, 2013)
- K130254: Prow Fusion (Oct 16, 2013)
- K130057: ESPIN (Feb 7, 2013)
- K120553: ESPIN (Aug 9, 2012)
- K112359: Prow Fusion (Nov 8, 2011)

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