510(k) K160969 ยท GDW Staple, Implantable
ShineMed Reloadable Open Cutting Stapler, ShineMed Curved Intraluminal Cutting Stapler
| Applicant | Shinemed, LLC, Winter Park FL, US |
| Decision | Substantially Equivalent, Dec 12, 2016 |
| Received | Apr 6, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160969
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.