Clearance Summary
Knee+ received FDA 510(k) clearance under submission number K230789, sponsored by Pixee Medical. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2023-04-21.
- Submission: K230789
- Applicant / Sponsor: Pixee Medical
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 2023-04-21
Classification & Regulation
This clearance is catalogued under FDA product code SBF and 21 CFR 882.4560, within the Neurology review panel as a Class II device.