K252623
- 510(k) number
- K252623
- Device name
- G7® Revision Acetabular System
- Applicant
- Zimmer, Inc. IN · US
- Product code
- LPH — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Po
- Decision date
- 2026-02-04
- Date received
- 2025-08-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K252623.pdf
Official FDA record: K252623
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.