# Peripheral Ave

- Location (FDA's records): Santa Rosa, CA
- FDA decisions: 2 (1998–1999): 2 510(k) clearances
- Product codes: FGE (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (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
- Medtronic Ave, Inc.: 4 (https://510kreport.com/company/medtronic-ave)
- Jomed, Inc.: 1 (https://510kreport.com/company/jomed)
- Edwards Lifesciences, LLC: 1 (https://510kreport.com/company/edwards-lifesciences)

## Its most-cited devices
- K983008: Peripheral Ave Stent System (1998), cited by 4
- K991533: Medtronic Ave Stent Delivery System - for Use in Biliary Indication (1999), cited by 2

## Recent decisions
- K991533: Medtronic Ave Stent Delivery System - for Use in Biliary Indication (Jul 29, 1999)
- K983008: Peripheral Ave Stent System (Nov 25, 1998)

Source page: https://510kreport.com/company/peripheral-ave