TRAXCESS 14 GUIDEWIRE— 510(k) K133725

Substantially Equivalent

MicroVention, Inc.

FDA 510(k) clearance K133725 for TRAXCESS 14 GUIDEWIRE, Substantially Equivalent on 2014-07-31. Applicant: MicroVention, Inc..

Clearance details

Applicant: MicroVention, Inc.
Product code: Code MOF
Advisory panel: Cardiovascular
Date received: 2013-12-06
Decision date: 2014-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tistin, CA, US

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Adverse events under product code MOF

product code MOF

Death: 6
Injury: 137
Total: 143

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.