510(k) K230492 · FMF Syringe, Piston
Avitus® Precision Autograft Delivery System
| Applicant | Avitus Orthopaedics, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jun 26, 2023 |
| Received | Feb 23, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230492
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.