FDA 510(k) Applications Submitted by ARTFX Medical
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K240889 | 04/01/2024 | ARTFX Lumbar PEEK Cages | ARTFX Medical |
| K240893 | 04/01/2024 | ARTFX MEDICAL Cervical PEEK Cages | ARTFX Medical |
| K242939 | 09/25/2024 | ARTFX Trauma Bone Plate and Screw System | ARTFX Medical |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact