IlluminOss Bone Stabilization System— 510(k) DEN160062

Unknown

Illminoss Medical, Inc.

FDA 510(k) clearance DEN160062 for IlluminOss Bone Stabilization System, Unknown on 2017-12-19. Applicant: Illminoss Medical, Inc..

Clearance details

Applicant: Illminoss Medical, Inc.
Product code: Code QAD
Advisory panel: Orthopedic
Date received: 2016-12-28
Decision date: 2017-12-19
Decision: Unknown
Clearance type: Direct
Location: East Providence, RI, US

View on FDA.gov ↗

Adverse events under product code QAD

product code QAD

Death: 13
Total: 13

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.