Last synced on 25 November 2022 at 11:04 pm

MODIFICATION TO: XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050501
510(k) Type
Special
Applicant
ABBOTT VASCULAR DEVICES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
3/14/2005
Days to Decision
14 days
Submission Type
Summary

MODIFICATION TO: XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050501
510(k) Type
Special
Applicant
ABBOTT VASCULAR DEVICES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
3/14/2005
Days to Decision
14 days
Submission Type
Summary