510(k) K150424 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
JuggerStitch Meniscal Repair Device
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, May 15, 2015 |
| Received | Feb 19, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150424
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.