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MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021729
510(k) Type
Special
Applicant
Sulzer Intratherapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
6/21/2002
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021729
510(k) Type
Special
Applicant
Sulzer Intratherapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
6/21/2002
Days to Decision
28 days
Submission Type
Summary