K241666
- 510(k) number
- K241666
- Device name
- EVOS Pelvic and Acetabular System
- Applicant
- Smith & Nephew TN · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2025-02-19
- Date received
- 2024-06-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K241666.pdf
Official FDA record: K241666
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.