K252781
- 510(k) number
- K252781
- Device name
- MSFX MIKRON PEEK CAGES
- Applicant
- Mikron Makina Sanayi VE Tic. Ltd. Sti. TR
- Product code
- ODP — Intervertebral Fusion Device With Bone Graft, Cervic
- Decision date
- 2025-12-19
- Date received
- 2025-09-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K252781.pdf
Official FDA record: K252781
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.