SPIDERFX EMBOLIC PROTECTION DEVICE— 510(k) K063204

Substantially Equivalent

Ev3, Inc.

FDA 510(k) clearance K063204 for SPIDERFX EMBOLIC PROTECTION DEVICE, Substantially Equivalent on 2006-11-14. Applicant: Ev3, Inc..

Clearance details

Applicant: Ev3, Inc.
Product code: Code NTE
Advisory panel: Cardiovascular
Date received: 2006-10-23
Decision date: 2006-11-14
Decision: Substantially Equivalent
Clearance type: Special
Location: Plymouth, MN, US

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Adverse events under product code NTE

product code NTE

Death: 28
Injury: 1,348
Malfunction: 771
Total: 2,147

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.