510(k) K241171 ยท OLO Orthopedic Stereotaxic Instrument
Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories
| Applicant | Stryker Leibinger GmbH & Co KG, Freiburg Baden-Wurttemberg, DE |
| Decision | Substantially Equivalent, Jul 25, 2024 |
| Received | Apr 26, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241171
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.