510(k) K110581 ยท FTM Mesh, Surgical
PROPATCH SOFT TISSUE REPAIR MATRIX
| Applicant | Cryolife, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Jan 10, 2012 |
| Received | Mar 1, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110581
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.