K233396
- 510(k) number
- K233396
- Device name
- Cannulated Screw System
- Applicant
- Smith & Nephew, Inc. TN · US
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2023-12-21
- Date received
- 2023-10-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K233396.pdf
Official FDA record: K233396
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.