K243838
- 510(k) number
- K243838
- Device name
- NEXXT MATRIXX® SI System
- Applicant
- Nexxt Spine IN · US
- Product code
- OUR — Sacroiliac Joint Fixation
- Decision date
- 2025-03-14
- Date received
- 2024-12-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K243838.pdf
Official FDA record: K243838
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.