K254233
- 510(k) number
- K254233
- Device name
- MEDPOR Customized Implant Kit
- Applicant
- Stryker Leibinger GmbH & Co KG DE
- Product code
- FWP — Prosthesis, Chin, Internal
- Decision date
- 2026-03-12
- Date received
- 2025-12-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K254233.pdf
Official FDA record: K254233
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.