STRYKER NAVIGATION SYSTEM - HIP MODULE— 510(k) K022365

Substantially Equivalent

Stryker Instruments

FDA 510(k) clearance K022365 for STRYKER NAVIGATION SYSTEM - HIP MODULE, Substantially Equivalent on 2003-01-22. Applicant: Stryker Instruments.

Clearance details

Applicant: Stryker Instruments
Product code: Code HAW
Advisory panel: Neurology
Date received: 2002-07-22
Decision date: 2003-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

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Adverse events under product code HAW

product code HAW

Death: 52
Injury: 1,083
Malfunction: 17,300
Total: 18,435

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.