510(k) K182104 ยท OLO Orthopedic Stereotaxic Instrument
NavLock Trackers, Robotic Reference Frame
| Applicant | Medtronic Navigation, Louisville CO, US |
| Decision | Substantially Equivalent, Nov 2, 2018 |
| Received | Aug 3, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182104
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 10, 2020 | Medtronic Navigation, Inc. NavLock Tracker *** Rx Only Terminated |
OLO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.