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FUSION VASCULAR GRAFT AND FUSION BIOLINE VASCULAR GRAFT

Page Type
Cleared 510(K)
510(k) Number
K131778
510(k) Type
Traditional
Applicant
MAQUET CARDIOVASCULAR LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2013
Days to Decision
150 days
Submission Type
Summary

FUSION VASCULAR GRAFT AND FUSION BIOLINE VASCULAR GRAFT

Page Type
Cleared 510(K)
510(k) Number
K131778
510(k) Type
Traditional
Applicant
MAQUET CARDIOVASCULAR LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2013
Days to Decision
150 days
Submission Type
Summary