# Spine-Tech, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 4 (1994–1998): 4 510(k) clearances
- Product codes: HRX (2), KWP (1), HWE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (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 that cite its devices most
- Sulzer Spine-Tech: 4 (https://510kreport.com/company/sulzer-spine-tech)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)
- Centerpulse Spine-Tech, Inc.: 1 (https://510kreport.com/company/centerpulse-spine-tech)
- Spinecraft, LLC: 1 (https://510kreport.com/company/spinecraft)

## Its most-cited devices
- K980288: Spine-Tech Silhouette Spinal Fixation System (1998), cited by 7

## Recent decisions
- K980288: Spine-Tech Silhouette Spinal Fixation System (Jul 29, 1998)
- K970040: Spine-Tech Bone Harvester (Feb 28, 1997)
- K951268: Spine-Tech Modified Laparoscopic Spinal Fusion Instrument System (Jul 31, 1995)
- K940913: Spine-Tech Laparoscopic Instrumentation System (Oct 4, 1994)

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