DeviceClearance

K250075

Substantially Equivalent

Medtronic Stedi Extra Support Guidewire

Applicant
Medtronic, Inc.
Product code
DQX
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Miinneapolis, MN, US
Download summary PDF View on FDA.gov ↗

Adverse events under product code DQX

product code DQX
Death
298
Injury
4,385
Malfunction
7,203
Other
5
Total
11,891

Source: openFDA MAUDE database, through . 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.