K031859

Substantially Equivalent

CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT

Applicant: Arthrosurface, Inc.
Product code: KWD
Advisory panel: Orthopedic
Date received: 2003-06-16
Decision date: 2004-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stoughton, MA, 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.