K234087
- 510(k) number
- K234087
- Device name
- restor3d TIDAL Lumbar Interbody Fusion System
- Applicant
- Restor3D NC · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2024-01-22
- Date received
- 2023-12-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.5 MB · U.S. public domain
Also available from FDA: K234087.pdf
Official FDA record: K234087
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.