K252326
- 510(k) number
- K252326
- Device name
- InterSpace GV Hip Spacer
- Applicant
- Tecres S.P.A. IT
- Product code
- KWL — Prosthesis, Hip, Hemi-, Femoral, Metal
- Decision date
- 2025-08-06
- Date received
- 2025-07-25
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252326.pdf
Official FDA record: K252326
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.