# Advanced Spine Technology, Inc.

- Location (FDA's records): Oakland, CA
- FDA decisions: 4 (1995–2006): 4 510(k) clearances
- Product codes: KWQ (2), MNI (1), MNH (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (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
- Advanced Med/Surg, Inc.: 1 (https://510kreport.com/company/advanced-med-surg)

## Firms that cite its devices most
- D.K.M. Co., Ltd.: 1 (https://510kreport.com/company/dkm)
- U&I Corporation: 1 (https://510kreport.com/company/u-i)
- Signus Medical, LLC: 1 (https://510kreport.com/company/signus-medical)
- Zavation, LLC: 1 (https://510kreport.com/company/zavation)

## Its most-cited devices
- K992147: Triple-Fix Spinal Fixation System (2000), cited by 3
- K993066: Window Cervical Dynamic Plate System (2000), cited by 1

## Recent decisions
- K062686: Universal Spinal Anterior Locking Plate System (Oct 5, 2006)
- K993066: Window Cervical Dynamic Plate System (Jun 7, 2000)
- K992147: Triple-Fix Spinal Fixation System (Feb 28, 2000)
- K951266: Amset R-F System (Nov 21, 1995)

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