K233972
- 510(k) number
- K233972
- Device name
- Camber Sacroiliac (SI) Fixation System
- Applicant
- Camber Spine Technologies PA · US
- Product code
- OUR — Sacroiliac Joint Fixation
- Decision date
- 2024-02-27
- Date received
- 2023-12-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K233972.pdf
Official FDA record: K233972
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.