510(k) K161221 ยท FTM Mesh, Surgical
Biodesign Sling, Biodesign Plastic Surgery Matrix, Biodesign Anal Fistula Plug
| Applicant | Cook Biotech Incorporated, West Lafayette IN, US |
| Decision | Substantially Equivalent, May 26, 2016 |
| Received | Apr 29, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161221
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.