510(k) K061113 ยท GWF Stimulator, Electrical, Evoked Response
ORTHOMON
| Applicant | Axon Systems, Inc., Hauppauge NY, US |
| Decision | Substantially Equivalent, May 23, 2006 |
| Received | Apr 21, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061113
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.