K252451
- 510(k) number
- K252451
- Device name
- EPORE® XO cup system
- Applicant
- Implantcast GmbH DE
- Product code
- OQI — Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polym
- Decision date
- 2026-04-24
- Date received
- 2025-08-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K252451.pdf
Official FDA record: K252451
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.