510(k) K191223 ยท OLO Orthopedic Stereotaxic Instrument
NAVIO
| Applicant | Blue Belt Technologies, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 28, 2019 |
| Received | May 7, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191223
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.