Last synced on 25 November 2022 at 11:04 pm

SENTINOL NITINOL BILLARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032025
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
9/25/2003
Days to Decision
87 days
Submission Type
Summary

SENTINOL NITINOL BILLARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032025
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
9/25/2003
Days to Decision
87 days
Submission Type
Summary