510(k) K080109— SYNTHES (USA) MODULAR BLADE PLATE SYSTEM

Substantially Equivalent

Synthes (Usa)

Clearance details

Applicant: Synthes (Usa)
Product code: Code KTW
Advisory panel: Orthopedic
Date received: 2008-01-15
Decision date: 2008-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Chester, PA, US

Adverse events under product code KTW

product code KTW

Injury: 220
Total: 220

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.