510(k) K123795 ยท GXY Electrode, Cutaneous
AXON-BUS PROSTHETIC SYSTEM
| Applicant | Otto Bock Austria, Vienna, AT |
| Decision | Substantially Equivalent, Jun 3, 2014 |
| Received | Dec 10, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123795
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.