MEDTRONIC MINIX & MINIX ST PULSE GENERATORS— 510(k) K930770

Substantially Equivalent

Medtronic Vascular

FDA 510(k) clearance K930770 for MEDTRONIC MINIX & MINIX ST PULSE GENERATORS, Substantially Equivalent on 1993-05-14. Applicant: Medtronic Vascular.

Clearance details

Applicant: Medtronic Vascular
Product code: Code DXY
Advisory panel: Cardiovascular
Date received: 1993-02-16
Decision date: 1993-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DXY

product code DXY

Death: 240
Injury: 2,328
Malfunction: 2,096
Total: 4,664

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.