510(k) K213125 ยท FTM Mesh, Surgical
PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology
| Applicant | Synovis Life Technologies. Inc. (A Subsidiary of Baxter, St. Paul MN, US |
| Decision | Substantially Equivalent, Oct 27, 2021 |
| Received | Sep 27, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213125
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.