510(k) K071300 ยท GXI Probe, Radiofrequency Lesion
MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE
| Applicant | Smith & Nephew, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jul 20, 2007 |
| Received | May 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071300
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.