Sulzer Intratherapeutics, Inc.
Sulzer Intratherapeutics, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2002.
Top product codes for Sulzer Intratherapeutics, Inc.
Recent clearances by Sulzer Intratherapeutics, Inc.
- K023243 — MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
- K021729 — MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
- K021563 — INTRACOIL SELF-EXPANDING PERIPHERAL STENT
- K020528 — INTRASTENT LD (LARGE DIAMETER) STENT
- K014136 — MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
- K011806 — PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
- K012347 — PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
- K012066 — PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
Data sourced from openFDA. This site is unofficial and independent of the FDA.