# Sulzer Intratherapeutics, Inc.

- Location (FDA's records): Saint Paul, MN
- FDA decisions: 8 (2001–2002): 8 510(k) clearances
- Product codes: FGE (7), JCT (1)
- Predicates its devices cite: 10 (3 its own); citations of its devices by later devices: 3 (3 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Intratherapeutics, Inc.: 7 (https://510kreport.com/company/intratherapeutics)

## Its most-cited devices
- K012066: Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (2001), cited by 2
- K012347: Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (2001), cited by 1

## Recent decisions
- K023243: Modification to Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (Dec 13, 2002)
- K021729: Modification to Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (Jun 21, 2002)
- K021563: Intracoil Self-Expanding Peripheral Stent (May 31, 2002)
- K020528: Intrastent LD (Large Diameter) Stent (Apr 16, 2002)
- K014136: Modification to Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (Jan 17, 2002)
- K011806: Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (Sep 7, 2001)
- K012347: Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (Aug 23, 2001)
- K012066: Protege Self-Expanding Nitinol Stent with Starport Delivery Technology (Aug 1, 2001)

Source page: https://510kreport.com/company/sulzer-intratherapeutics