510(k) K171253— Streamline 6491 Unipolar Pediatric Temporary Pacing Lead, Streamline 6492 Unipolar Temporary Pacing Lead, Streamline 6495 Bipolar Temporary Myocardial Pacing Lead, Streamline 6500 Unipolar Temporary Myocardial Pacing Lead

Substantially Equivalent

Medtronic

Clearance details

Applicant: Medtronic
Product code: Code LDF
Advisory panel: Cardiovascular
Date received: 2017-04-28
Decision date: 2017-05-25
Decision: Substantially Equivalent
Clearance type: Special
Location: Santa Ana, CA, US

Adverse events under product code LDF

product code LDF

Death: 19
Injury: 188
Malfunction: 694
Other: 1
Total: 902

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.