K233744
- 510(k) number
- K233744
- Device name
- Curiteva Porous PEEK Lumbar Interbody Fusion System
- Applicant
- Curiteva, Inc. AL · US
- Product code
- MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
- Decision date
- 2024-01-18
- Date received
- 2023-11-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K233744.pdf
Official FDA record: K233744
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.