510(k) K013553 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
PRE-LOADED ULTRAFIX RC
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Dec 19, 2001 |
| Received | Oct 25, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013553
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.