MVR Venous Reservoir Bag 800 mL; MVR Venous Reservoir Bag 1600 mL; MVR Venous Reservoir Bag with Cortiva BioActive
Summary
Medtronic Cardiac Surgery received 510(k) clearance for MVR Venous Reservoir Bag 800 mL; MVR Venous Reservoir Bag 1600 mL; MVR Venous Reservoir Bag with Cortiva BioActive Surface 800 mL; MVR Venous Reservoir Bag with Cortiva BioActive Surface 1600 mL, a DTN device. Cleared on 2024-05-15.
Details
Source
510(k) Clearance
External ID
K241053
Action Date
2024-05-15
Status
Special
Category
device
Product Code
DTN
Product Description
MVR Venous Reservoir Bag 800 mL; MVR Venous Reservoir Bag 1600 mL; MVR Venous Reservoir Bag with Cortiva BioActive Surface 800 mL; MVR Venous Reservoir Bag with Cortiva BioActive Surface 1600 mL. Product code: DTN.
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Medtronic Cardiac Surgery have FDA actions?
This is the only FDA action we have on record for Medtronic Cardiac Surgery in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K241053" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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