510(k) K053461 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
EZLOC FEMORAL FIXATION DEVICE
| Applicant | Arthrotek, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 3, 2006 |
| Received | Dec 13, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053461
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.