Artfx Medical
FDA Regulatory Profile
Artfx Medical appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Dec 23, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242939 | ARTFX Trauma Bone Plate and Screw System | Dec 23, 2024 |
| K240889 | ARTFX Lumbar PEEK Cages | Oct 2, 2024 |
| K240893 | ARTFX MEDICAL Cervical PEEK Cages | Jun 28, 2024 |
| K212220 | ArtFX Spinal Fixation System | Apr 20, 2023 |
| K211718 | Venus Cervical Plate System | Jun 28, 2022 |