STRYKER MMF SCREW— 510(k) K050535

Substantially Equivalent

Stryker Instruments

FDA 510(k) clearance K050535 for STRYKER MMF SCREW, Substantially Equivalent on 2005-03-17. Applicant: Stryker Instruments.

Clearance details

Applicant: Stryker Instruments
Product code: Code DZL
Advisory panel: Dental
Date received: 2005-03-02
Decision date: 2005-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

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.