K232468
- 510(k) number
- K232468
- Device name
- SC Medica FFX
- Applicant
- Sc Medica FR
- Product code
- MRW — System, Facet Screw Spinal Device
- Decision date
- 2024-05-09
- Date received
- 2023-08-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 1.3 MB · U.S. public domain
Also available from FDA: K232468.pdf
Official FDA record: K232468
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.