510(k) K122791 ยท GXQ Dura Substitute
LYOPLANT ONLAY
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jun 4, 2013 |
| Received | Sep 12, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122791
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.