K233949
- 510(k) number
- K233949
- Device name
- ACCORD Cable System
- Applicant
- Smith & Nephew, Inc. TN · US
- Product code
- JDQ — Cerclage, Fixation
- Decision date
- 2024-03-13
- Date received
- 2023-12-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K233949.pdf
Official FDA record: K233949
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.