# Vertelink Corporation

- Location (FDA's records): Mission Viejo, CA
- FDA decisions: 3 (2003–2003): 3 510(k) clearances
- Product codes: KWQ (1), EZN (1), DYB (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)

## Firms that cite its devices most
- Medtronic Vertelink, Inc.: 1 (https://510kreport.com/company/medtronic-vertelink)

## Its most-cited devices
- K032102: Vertelink Kobra Spinal Fixation System (2003), cited by 1

## Recent decisions
- K032102: Vertelink Kobra Spinal Fixation System (Dec 12, 2003)
- K030734: Pathway Access Sheath Catheter (Sep 10, 2003)
- K030662: Pathway Access Sheath Catheter (Sep 3, 2003)

Source page: https://510kreport.com/company/vertelink