510(k) K240484 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MSFX Mikron Cervical Anterior Plate System
| Applicant | Mikron Makina Sanayi VE Ticaret Ltd. Sti., Ivedik, TR |
| Decision | Substantially Equivalent, Apr 17, 2024 |
| Received | Feb 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240484
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.