Clearance Summary
Juliet® Ti LL Lumbar Interbody Device received FDA 510(k) clearance under submission number K241321, sponsored by Spineart SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-07-18.
- Submission: K241321
- Applicant / Sponsor: Spineart SA
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3080
- Decision date: 2024-07-18
Classification & Regulation
This clearance is catalogued under FDA product code OVD and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.