510(k) K181559 ยท PDQ Neurosurgical Nerve Locator
Neurosign V4 Intraoperative Nerve Monitor
| Applicant | Magstim Company, Ltd., Whitland, GB |
| Decision | Substantially Equivalent, Nov 9, 2018 |
| Received | Jun 13, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181559
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 23, 2020 | The Magstim Company Limited Neurosign V4 Intraoperative Nerve monitor family of devices. Terminated |
PDQ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.