Last synced on 25 November 2022 at 11:04 pm

MODIFICATION TO:XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM, MODELS 14819, 14820, 14821, 14822, 14822

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032929
510(k) Type
Special
Applicant
ABBOTT VASCULAR INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/22/2003
Days to Decision
30 days
Submission Type
Summary

MODIFICATION TO:XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM, MODELS 14819, 14820, 14821, 14822, 14822

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032929
510(k) Type
Special
Applicant
ABBOTT VASCULAR INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/22/2003
Days to Decision
30 days
Submission Type
Summary