K242674
- 510(k) number
- K242674
- Device name
- Freedom Posterior Cervical Screws
- Applicant
- Signature Orthopaedics Pty, Ltd. AU
- Product code
- NKG — Posterior Cervical Screw System
- Decision date
- 2025-05-13
- Date received
- 2024-09-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242674.pdf
Official FDA record: K242674
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.