510(k) K911717 ยท LZN Cement Obturator
ADG INTRAMEDULLARY BONE PLUG - VENTED
| Applicant | American Design Group, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Sep 4, 1991 |
| Received | Apr 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911717
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.