K243571
- 510(k) number
- K243571
- Device name
- Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained Liners
- Applicant
- Zimmer Biomet IN · US
- Product code
- JDI — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Ce
- Decision date
- 2025-07-31
- Date received
- 2024-11-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K243571.pdf
Official FDA record: K243571
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.