STRYKER VENOM ELECTRODES AND CANNULAE— 510(k) K123178

Name: FDA 510(k) clearance K123178
Creator: U.S. Food and Drug Administration
Published: 2013-03-28

Substantially Equivalent

Stryker Instruments, Instruments Div.

FDA 510(k) clearance K123178 for STRYKER VENOM ELECTRODES AND CANNULAE, Substantially Equivalent on 2013-03-28. Applicant: Stryker Instruments, Instruments Div.. Device class: 2.

Clearance details

Applicant: Stryker Instruments, Instruments Div.
Product code: Code GXI
Device class: Class 2
Regulation: 21 CFR 882.4725
Advisory panel: Neurology
Date received: 2012-10-09
Decision date: 2013-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GXI

product code GXI

Death: 3
Injury: 171
Total: 174

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.