510(k) K183513 ยท GXQ Dura Substitute
XenoSure Dura Biologic Patch
| Applicant | LeMaitre Vascular, Inc., Burlington MA, US |
| Decision | Substantially Equivalent, Jun 13, 2019 |
| Received | Dec 18, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183513
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.