BIOCERAM AZUL® HEAD— 510(k) K243444

Substantially Equivalent

Kyocera Corporation

FDA 510(k) clearance K243444 for BIOCERAM AZUL® HEAD, Substantially Equivalent on 2024-12-05. Applicant: Kyocera Corporation.

Clearance details

Applicant: Kyocera Corporation
Product code: Code LZO
Advisory panel: Orthopedic
Date received: 2024-11-06
Decision date: 2024-12-05
Decision: Substantially Equivalent
Clearance type: Special
Location: Kyoto, JP

Download summary PDF View on FDA.gov ↗

Adverse events under product code LZO

product code LZO

Death: 17
Injury: 12,942
Malfunction: 1,756
Total: 14,715

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.