NON-INVASIVE PATIENT FIXATION SYSTEM— 510(k) K023449

Substantially Equivalent

Stryker Leibinger

FDA 510(k) clearance K023449 for NON-INVASIVE PATIENT FIXATION SYSTEM, Substantially Equivalent on 2003-01-13. Applicant: Stryker Leibinger.

Clearance details

Applicant: Stryker Leibinger
Product code: Code IYE
Advisory panel: Radiology
Date received: 2002-10-15
Decision date: 2003-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

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Adverse events under product code IYE

product code IYE

Malfunction: 455
Other: 3
Total: 458

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.