K895702

Substantially Equivalent

KDR ACETABULAR COMPONENT

Applicant: Osteonics Corp.
Product code: LWJ
Advisory panel: Orthopedic
Date received: 1989-09-22
Decision date: 1989-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Allendale, NJ, US

Adverse events under product code LWJ

product code LWJ

Injury: 544
Total: 544

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.