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MODIFICATION TO CARDICA C-PORT XA DISTAL ANASTOMOSIS SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090872
510(k) Type
Special
Applicant
Cardica, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2009
Days to Decision
22 days
Submission Type
Summary

MODIFICATION TO CARDICA C-PORT XA DISTAL ANASTOMOSIS SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090872
510(k) Type
Special
Applicant
Cardica, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2009
Days to Decision
22 days
Submission Type
Summary