K240783
- 510(k) number
- K240783
- Device name
- Anthology Hip Stems; CPCS Hip Stems; Femoral Heads; R3 Acetabular Liners; Spectron Hip Stems; Synergy Hip Stems
- Applicant
- Smith & Nephew, Inc. TN · US
- Product code
- JDI — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Ce
- Decision date
- 2024-10-21
- Date received
- 2024-03-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K240783.pdf
Official FDA record: K240783
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.