510(k) K162707 ยท GDW Staple, Implantable
Single Use Circular Stapler, Single Use Hemorrhoidal Circular Stapler, Single Patient Use Linear Stapler and Reload, Single Patient Use Linear Cutter and Reload, Single Patient Use Endo Cutter and Reload, Single Patient Use Transverse Cutter and Reload
| Applicant | Golden Stapler Surgical Co., Ltd., Changzhou, CN |
| Decision | Substantially Equivalent, Jul 14, 2017 |
| Received | Sep 28, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162707
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.