510(k) K003906 ยท FTL Mesh, Surgical, Polymeric
MODIFICATION TO FLUROTEX SURGICAL MESH
| Applicant | Bridger Biomed, Inc., Bozeman MT, US |
| Decision | Substantially Equivalent, Jan 26, 2001 |
| Received | Dec 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003906
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.