K233899
- 510(k) number
- K233899
- Device name
- Knee+
- Applicant
- Pixee Medical FR
- Product code
- SBF — Orthopedic Augmented Reality
- Decision date
- 2024-03-08
- Date received
- 2023-12-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
510(k) Summary (official FDA PDF): K233899.pdf
Official FDA record: K233899
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.