510(k) K133354 ยท JDQ Cerclage, Fixation
PERI-PROSTHETIC CABLE SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 27, 2014 |
| Received | Oct 31, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133354
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.