CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365— 510(k) K023684

Substantially Equivalent

Vilex, Inc.

FDA 510(k) clearance K023684 for CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365, Substantially Equivalent on 2004-03-01. Applicant: Vilex, Inc..

Clearance details

Applicant: Vilex, Inc.
Product code: 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

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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.