# Sulzermedica

- Location (FDA's records): Austin, TX
- FDA decisions: 6 (1997–2000): 5 510(k) clearances and 1 original PMA approval
- Product codes: DSY (3), MBD (1), JDI (1), KWA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Vascutek, Ltd.: 2 (https://510kreport.com/company/vascutek)
- Zimmer, Inc.: 2 (https://510kreport.com/company/zimmer)
- Veryan Medical Limited: 1 (https://510kreport.com/company/veryan-medical)
- Centerpulse Orthopedics, Inc.: 1 (https://510kreport.com/company/centerpulse-orthopedics)

## Its most-cited devices
- P940002: Natural-Knee (R) and Natural Knee (R)II W/Csti (TM) (1997), cited by 2
- K992832: Sulzer Vascutek Eptfe Vascular Prosthesis (1999), cited by 2
- K002324: Modified to Modular FR Severe Bone Loss Trauma (2000), cited by 1
- K990503: Sulzer Vascutek Gelsoft Vascular Prosthesis (1999), cited by 1

## Recent decisions
- K002324: Modified to Modular FR Severe Bone Loss Trauma (Aug 24, 2000)
- K993667: Sulzer Vascutek Sealptfe Vascular Prosthesis (Jan 28, 2000)
- K990503: Sulzer Vascutek Gelsoft Vascular Prosthesis (Dec 9, 1999)
- K993569: Apr Metasul Acetabular Insert (Dec 1, 1999)
- K992832: Sulzer Vascutek Eptfe Vascular Prosthesis (Nov 19, 1999)
- P940002: Natural-Knee (R) and Natural Knee (R)II W/Csti (TM) (Mar 21, 1997)

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