510(k) K013120 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
PERCUTANEOUS INTRODUCER SET, MODEL 042294 AND KIT MODEL 3550-18
| Applicant | Medamicus, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 24, 2002 |
| Received | Sep 18, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013120
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.