K232173
- 510(k) number
- K232173
- Device name
- Ascend VBR System, Ascend NanoTec VBR System
- Applicant
- Alphatec Spine, Inc. CA · US
- Product code
- MQP — Spinal Vertebral Body Replacement Device
- Decision date
- 2023-10-06
- Date received
- 2023-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K232173.pdf
Official FDA record: K232173
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.