# N Spine, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 3 (2006–2007): 3 510(k) clearances
- Names in FDA's records: N Spine, Inc. (2); N-Spine, Inc. (1)
- Product codes: NQP (2), MNH (1)
- Predicates its devices cite: 12 (2 its own); citations of its devices by later devices: 4 (2 its own)
- Recalls linked to its devices: 11 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Scien'Tx USA, Inc.: 2 (https://510kreport.com/company/scien-tx-usa)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Depuy Motech: 1 (https://510kreport.com/company/depuy-motech)
- Depuyacromed: 1 (https://510kreport.com/company/depuyacromed)
- Buckman Co., Inc.: 1 (https://510kreport.com/company/buckman)
- Endocardial Solutions, Inc.: 1 (https://510kreport.com/company/endocardial-solutions)
- U&I Corp., America: 1 (https://510kreport.com/company/u-i-america)

## Firms that cite its devices most
- Bk Meditech, Co., Ltd.: 1 (https://510kreport.com/company/bk-meditech)
- Vertiflex, Inc.: 1 (https://510kreport.com/company/vertiflex)

## Its most-cited devices
- K053623: Nfix Fusion System (2006), cited by 2
- K061774: Nfix II Pedicle Screw System (2006), cited by 2

## Recent decisions
- K072685: Ngarde System (Oct 19, 2007)
- K061774: Nfix II Pedicle Screw System (Dec 13, 2006)
- K053623: Nfix Fusion System (Jul 12, 2006)

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