510(k) K223445 ยท GXQ Dura Substitute
ArtiFascia
| Applicant | Nurami Medical , Ltd., Haifa, IL |
| Decision | Substantially Equivalent, Aug 10, 2023 |
| Received | Nov 14, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223445
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.