KNEEALIGN SYSTEM— 510(k) K103829

Substantially Equivalent

Orthalign, Inc.

FDA 510(k) clearance K103829 for KNEEALIGN SYSTEM, Substantially Equivalent on 2011-04-04. Applicant: Orthalign, Inc..

Clearance details

Applicant: Orthalign, Inc.
Product code: Code OLO
Advisory panel: Neurology
Date received: 2010-12-30
Decision date: 2011-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newport Beach, CA, US

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.