MULLER TYPE ACETABULAR CUP— 510(k) K900257

Substantially Equivalent

Lima Intl. Corp.

FDA 510(k) clearance K900257 for MULLER TYPE ACETABULAR CUP, Substantially Equivalent on 1990-04-18. Applicant: Lima Intl. Corp..

Clearance details

Applicant: Lima Intl. Corp.
Product code: Code JDI
Advisory panel: Orthopedic
Date received: 1990-01-17
Decision date: 1990-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: E Providence, RI, US

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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.