510(k) K120824 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
3.9MM REELX STT SUTURE ANCHOR SYSTEM
| Applicant | Stryker Corp., Denver CO, US |
| Decision | Substantially Equivalent, Jul 18, 2012 |
| Received | Mar 19, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120824
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.