510(k) K960481 ยท FTL Mesh, Surgical, Polymeric
SOFT TISSUE AUGMENTATION TUBE
| Applicant | Tissue Technologies, Inc., San Francisco CA, US |
| Decision | Substantially Equivalent, Apr 1, 1996 |
| Received | Feb 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960481
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.