510(k) K081348 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD
| Applicant | TriMed, Inc., Valencia CA, US |
| Decision | Substantially Equivalent, Oct 17, 2008 |
| Received | May 14, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081348
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.