510(k) K133938 ยท GDW Staple, Implantable
ENDO GIA REINFORCED RELOAD WITH TRI-STAPLE TECHNOLOGY
| Applicant | Covidien, Mansfield MA, US |
| Decision | Substantially Equivalent, Jan 22, 2014 |
| Received | Dec 23, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133938
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.