MAX-FACE MAXILLOFACIAL OSTEOSYNTHESIS SYSTEM— 510(k) K073307

Substantially Equivalent

Bio-Technology USA, Inc.

FDA 510(k) clearance K073307 for MAX-FACE MAXILLOFACIAL OSTEOSYNTHESIS SYSTEM, Substantially Equivalent on 2008-10-29. Applicant: Bio-Technology USA, Inc..

Clearance details

Applicant: Bio-Technology USA, Inc.
Product code: Code JEY
Advisory panel: Dental
Date received: 2007-11-23
Decision date: 2008-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code JEY

product code JEY

Injury: 1,542
Malfunction: 2,292
Total: 3,834

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.