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DLP Silicone Coronary Artery Ostial Cannulae

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231206
510(k) Type
Special
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2023
Days to Decision
224 days
Submission Type
Summary

DLP Silicone Coronary Artery Ostial Cannulae

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231206
510(k) Type
Special
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2023
Days to Decision
224 days
Submission Type
Summary