510(k) K002071 ยท FTL Mesh, Surgical, Polymeric
SOFTFORM SOFT TISSUE AUGMENTATION TUBE WITH INSERTION TOOL MODIFICATIONS FOR STRANDS AND SUTURE HOLES
| Applicant | Tissue Technologies, Inc., San Francisco CA, US |
| Decision | Substantially Equivalent, Jul 24, 2000 |
| Received | Jul 7, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002071
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.