Sprinter Legend Rapid Exchange Balloon Dilatation Catheter— 510(k) K251970

Substantially Equivalent

Medtronic, Ireland

FDA 510(k) clearance K251970 for Sprinter Legend Rapid Exchange Balloon Dilatation Catheter, Substantially Equivalent on 2026-01-17. Applicant: Medtronic, Ireland.

Clearance details

Applicant: Medtronic, Ireland
Product code: Code LOX
Advisory panel: Cardiovascular
Date received: 2025-06-26
Decision date: 2026-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Galway, IE

Download summary PDF View on FDA.gov ↗

Adverse events under product code LOX

product code LOX

Death: 190
Injury: 1,498
Malfunction: 9,670
Total: 11,358

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.