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DURAMAX .018 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K032436
510(k) Type
Traditional
Applicant
AVANTEC VASCULAR CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
2/4/2004
Days to Decision
181 days
Submission Type
Summary

DURAMAX .018 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K032436
510(k) Type
Traditional
Applicant
AVANTEC VASCULAR CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
2/4/2004
Days to Decision
181 days
Submission Type
Summary