K243444
- 510(k) number
- K243444
- Device name
- BIOCERAM AZUL® HEAD
- Applicant
- Kyocera Corporation JP
- Product code
- LZO — Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Pol
- Decision date
- 2024-12-05
- Date received
- 2024-11-06
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K243444.pdf
Official FDA record: K243444
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.