Last synced on 25 January 2026 at 3:41 am

INTRASTENT 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
K003040
510(k) Type
Traditional
Applicant
Intratherapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
12/28/2000
Days to Decision
90 days
Submission Type
Summary

INTRASTENT 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
K003040
510(k) Type
Traditional
Applicant
Intratherapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
12/28/2000
Days to Decision
90 days
Submission Type
Summary