510(k) K220593 ยท OLO Orthopedic Stereotaxic Instrument
Spine Guidance Software, Stryker Q Guidance System
| Applicant | Stryker Leibinger GmbH & Co KG, Freiburg, DE |
| Decision | Substantially Equivalent, May 27, 2022 |
| Received | Mar 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220593
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.