510(k) K170242 · GXD Generator, Lesion, Radiofrequency
MultiGen 2 RF Generator System
| Applicant | Stryker Corporation, Kalamazoo MI, US |
| Decision | Substantially Equivalent, May 25, 2017 |
| Received | Jan 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170242
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.