K241175
- 510(k) number
- K241175
- Device name
- MiRus MoRe Lumbar Plating System
- Applicant
- MiRus, LLC GA · US
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2024-05-17
- Date received
- 2024-04-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K241175.pdf
Official FDA record: K241175
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.