K231134
- 510(k) number
- K231134
- Device name
- VerteLoc Spinal System
- Applicant
- Signature Orthopaedics Pty, Ltd. AU
- Product code
- MQP — Spinal Vertebral Body Replacement Device
- Decision date
- 2024-02-13
- Date received
- 2023-04-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K231134.pdf
Official FDA record: K231134
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.