K232256
- 510(k) number
- K232256
- Device name
- Alcantara Thoracolumbar Plate System
- Applicant
- Camber Spine Technologies, LLC PA · US
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2024-04-16
- Date received
- 2023-07-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K232256.pdf
Official FDA record: K232256
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.