K140286

Substantially Equivalent

OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER

Applicant: Cordis, A Johnson & Johnson Co.
Product code: DTK
Advisory panel: Cardiovascular
Date received: 2014-02-05
Decision date: 2014-03-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Fremont, CA, US

Adverse events under product code DTK

product code DTK

Death: 208
Injury: 11,286
Malfunction: 3,002
Total: 14,496

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.