K240113
- 510(k) number
- K240113
- Device name
- CORIOGRAPH Knee Pre-Op Plan
- Applicant
- Smith & Nephew, Inc. TN · US
- Product code
- PBF — Orthopaedic Surgical Planning And Instrument Guides
- Decision date
- 2024-03-18
- Date received
- 2024-01-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K240113.pdf
Official FDA record: K240113
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.