K252930
- 510(k) number
- K252930
- Device name
- AQUA Laminoplasty Systems
- Applicant
- ZheJiang Decans Medical Devices Co., Ltd. CN
- Product code
- NQW — Orthosis, Spine, Plate, Laminoplasty, Metal
- Decision date
- 2026-05-27
- Date received
- 2025-09-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K252930.pdf
Official FDA record: K252930
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.