Medtronic Core Valve, LLC

FDA Regulatory Profile

Medtronic Core Valve, LLC has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
May 3, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K181001Medtronic Confida Brecker GuidewireMay 3, 2018
K150465Medtronic Confida Brecker GuidewireAug 3, 2015