510(k) K060397 ยท GXI Probe, Radiofrequency Lesion
RF LESION CANNULA, RF THERMOLESION CANNULA, THERMOLESION CANNULA, X-RAY CONTRAST CANNULA, CANNULA, FACET DENERATION NEED
| Applicant | PAJUNK GmbH Medizintechnologie, Geisingen, DE |
| Decision | Substantially Equivalent, Aug 31, 2006 |
| Received | Feb 15, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060397
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.