K233215
- 510(k) number
- K233215
- Device name
- icotec Anterior Cervical Plate System
- Applicant
- Icotec AG CH
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2024-05-17
- Date received
- 2023-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.8 MB · U.S. public domain
Also available from FDA: K233215.pdf
Official FDA record: K233215
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.