Last synced on 30 May 2025 at 11:05 pm

MYOtherm XP Cardioplegia Delivery System with Cortiva BioActive Surface, MYOtherm XP Cardioplegia Delivery System Uncoated

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240190
510(k) Type
Special
Applicant
Medtronic
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2024
Days to Decision
30 days
Submission Type
Summary

MYOtherm XP Cardioplegia Delivery System with Cortiva BioActive Surface, MYOtherm XP Cardioplegia Delivery System Uncoated

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240190
510(k) Type
Special
Applicant
Medtronic
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2024
Days to Decision
30 days
Submission Type
Summary