K243693
- 510(k) number
- K243693
- Device name
- NEO Pedicle Screw System
- Applicant
- Neo Medical SA CH
- Product code
- NKB — Thoracolumbosacral Pedicle Screw System
- Decision date
- 2024-12-23
- Date received
- 2024-11-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K243693.pdf
Official FDA record: K243693
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.