510(k) K223108 ยท OLO Orthopedic Stereotaxic Instrument
TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear)
| Applicant | Medos International SARL, Lelocle, CH |
| Decision | Substantially Equivalent, Jan 19, 2023 |
| Received | Sep 30, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223108
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.