510(k) K251970

Device
Sprinter Legend Rapid Exchange Balloon Dilatation Catheter
Applicant
Medtronic, Ireland
510(k) number
K251970
Product code
LOX
Decision
Substantially Equivalent (SESE)
Decision date
2026-01-17
Date received
2025-06-26
Regulation
870.5100
Classification name
Catheters, Transluminal Coronary Angioplasty, Percutaneous
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Michelle Greaney
Address
Parkmore Business Park W. Galway IE H91VY19 H91VY19

FDA Registration Numbers

Source Documents

510(k) summary PDF

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