K243137
- 510(k) number
- K243137
- Device name
- Curiteva Porous PEEK Laminoplasty System
- Applicant
- Curiteva, Inc. AL · US
- Product code
- NQW — Orthosis, Spine, Plate, Laminoplasty, Metal
- Decision date
- 2024-10-28
- Date received
- 2024-09-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K243137.pdf
Official FDA record: K243137
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.