MICRUS MICROCATHETER, MODEL COURIER 270— 510(k) K092702

Clearance details

Applicant

Micrus Endovascular Corporation

Product code

Code DQO

Device class

Class 2

Regulation

21 CFR 870.1200

Advisory panel

Cardiovascular

Date received

2009-09-02

Decision date

2009-11-20

Decision

Substantially Equivalent

Clearance type

Special

Location

San Jose, CA, US

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• K083922 — MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-002009-05-06
• K090274 — MICRUS ONE 2 ONE GUIDEWIRE AND SOFT GUIDEWIRE2009-03-03

Death

35

Injury

993

Malfunction

1,772

Other

5

Total

2,805

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 →