Spine & Trauma Navigation— 510(k) K191285

Substantially Equivalent

Brainlab AG

FDA 510(k) clearance K191285 for Spine & Trauma Navigation, Substantially Equivalent on 2019-06-11. Applicant: Brainlab AG.

Clearance details

Applicant: Brainlab AG
Product code: Code OLO
Advisory panel: Neurology
Date received: 2019-05-13
Decision date: 2019-06-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Munich, DE

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.