K242315
- 510(k) number
- K242315
- Device name
- Resolve Modular Revision Hip Stem
- Applicant
- United Orthopedic Corporation TW
- Product code
- MEH — Prosthesis, Hip, Semi-Constrained, Uncemented, Metal
- Decision date
- 2025-05-01
- Date received
- 2024-08-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K242315.pdf
Official FDA record: K242315
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.