Last synced on 2 December 2022 at 11:04 pm

DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML0718-135, DML0818-80, DML0818-135, DML0918-80, DML0918-135, DML

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030638
510(k) Type
Traditional
Applicant
AVANTEC VASCULAR CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
7/9/2003
Days to Decision
131 days
Submission Type
Summary

DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML0718-135, DML0818-80, DML0818-135, DML0918-80, DML0918-135, DML

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030638
510(k) Type
Traditional
Applicant
AVANTEC VASCULAR CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
7/9/2003
Days to Decision
131 days
Submission Type
Summary