INTAI Surgery Navigation System— 510(k) K180523

Substantially Equivalent

Intai Technology Corporation

FDA 510(k) clearance K180523 for INTAI Surgery Navigation System, Substantially Equivalent on 2019-09-20. Applicant: Intai Technology Corporation.

Clearance details

Applicant: Intai Technology Corporation
Product code: Code OLO
Advisory panel: Neurology
Date received: 2018-02-27
Decision date: 2019-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taichung, TW

Download summary PDF View on FDA.gov ↗

Adverse events under product code OLO

product code OLO

Death: 11
Injury: 2,799
Malfunction: 11,105
Other: 1
Total: 13,916

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.