Sulzer Intratherapeutics, Inc.
FDA 510(k) medical device clearances.
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.