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GUIDANT AXIUS CORONARY SHUNT

Page Type
Cleared 510(K)
510(k) Number
K010117
510(k) Type
Traditional
Applicant
CARDIOTHORACIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2001
Days to Decision
78 days
Submission Type
Summary

GUIDANT AXIUS CORONARY SHUNT

Page Type
Cleared 510(K)
510(k) Number
K010117
510(k) Type
Traditional
Applicant
CARDIOTHORACIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2001
Days to Decision
78 days
Submission Type
Summary