ARTHOPOR-ACETABULAR COMPONENT— 510(k) K844050

Substantially Equivalent for Some Indications

Joint Medical Products Corp.

FDA 510(k) clearance K844050 for ARTHOPOR-ACETABULAR COMPONENT, Substantially Equivalent for Some Indications on 1985-12-06. Applicant: Joint Medical Products Corp..

Clearance details

Applicant: Joint Medical Products Corp.
Product code: Code JDI
Advisory panel: Orthopedic
Date received: 1984-10-17
Decision date: 1985-12-06
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Stamford, CT, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code JDI

product code JDI

Death: 65
Injury: 12,943
Malfunction: 1,681
Total: 14,689

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.