510(k) K161757 ยท GDW Staple, Implantable
Single Use Curved Cutters, Single Use Circular Staplers, Single Use Linear Cutters and Reloads, Single Use Endoscopic Linear Cutters and Reloads, Single Use Hemorrhoidal Staplers, Single Use Linear Staplers and Reloads
| Applicant | Victor Medical Instruments Co., Ltd., Changzhou, CN |
| Decision | Substantially Equivalent, Dec 5, 2016 |
| Received | Jun 27, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161757
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.