K233507
- 510(k) number
- K233507
- Device name
- EVOLUTION® Tibial Cones
- Applicant
- Microport Orthopedics, Inc. TN · US
- Product code
- MBH — Prosthesis, Knee, Patello/Femorotibial, Semi-Constra
- Decision date
- 2024-01-18
- Date received
- 2023-10-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233507.pdf
Official FDA record: K233507
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.