K242939
- 510(k) number
- K242939
- Device name
- ARTFX Trauma Bone Plate and Screw System
- Applicant
- Artfx Medical FL · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2024-12-23
- Date received
- 2024-09-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K242939.pdf
Official FDA record: K242939
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.