K050606

Substantially Equivalent

SYNTHES 1.0MM TI. CORTEX, SELF-DRILLING SCREWS (CARNIOFACIAL)

Applicant: Synthes (Usa)
Product code: DZL
Advisory panel: Dental
Date received: 2005-03-10
Decision date: 2005-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Chester, PA, US

Adverse events under product code DZL

product code DZL

Injury: 168
Total: 168

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.