K043073

Substantially Equivalent

PROCOTYL-E ACETABULAR SYSTEM

Applicant: Wrightmedicaltechnologyinc
Product code: KWA
Advisory panel: Orthopedic
Date received: 2004-11-08
Decision date: 2005-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TN, US

Adverse events under product code KWA

product code KWA

Death: 38
Injury: 10,439
Malfunction: 1,862
Total: 12,339

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.