FDA-Device2024-02-21Class II
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Stryker, Inc.
Hazard
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
Sold states
US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.
Affected count
11 units
Manufactured in
4870 West 2100 South, N/A, Salt Lake City, UT, United States
Products
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1084-2024Don't want to check this manually?
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