K241321
- 510(k) number
- K241321
- Device name
- Juliet® Ti LL Lumbar Interbody Device
- Applicant
- Spineart SA CH
- Product code
- OVD — Intervertebral Fusion Device With Integrated Fixatio
- Decision date
- 2024-07-18
- Date received
- 2024-05-10
- 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: K241321.pdf
Official FDA record: K241321
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.