510(k) K121124 ยท FMF Syringe, Piston
ARTHREX MIXING AND DELIVERY SYSTEM
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, May 16, 2012 |
| Received | Apr 13, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121124
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.