510(k) K141812 ยท GZI Stimulator, Neuromuscular, External Functional
MYGAIT STIMULATION SYSTEM
| Applicant | Otto Bock Healthcare Products GmbH, Vienna, AT |
| Decision | Substantially Equivalent, Apr 2, 2015 |
| Received | Jul 7, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141812
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.