510(k) K113805 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
FIXATE TISSUE BAND
| Applicant | Anulex Technologies, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Feb 23, 2012 |
| Received | Dec 23, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113805
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.