K023684

Substantially Equivalent

CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365

Applicant: Vilex, Inc.
Product code: KWD
Advisory panel: Orthopedic
Date received: 2002-11-01
Decision date: 2004-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasant Hills, PA, US

Adverse events under product code KWD

product code KWD

Injury: 164
Total: 164

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.