K240938
- 510(k) number
- K240938
- Device name
- The Optimotion Blue Plus Knee System
- Applicant
- Optimotion Implants, LLC FL · US
- Product code
- MBH — Prosthesis, Knee, Patello/Femorotibial, Semi-Constra
- Decision date
- 2024-06-27
- Date received
- 2024-04-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K240938.pdf
Official FDA record: K240938
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.