510(k) K172603 ยท GXQ Dura Substitute
Cerafix Dura Substitute
| Applicant | Acera Surgical, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Nov 27, 2017 |
| Received | Aug 30, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172603
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.