510(k) K233542 ยท OLO Orthopedic Stereotaxic Instrument
Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System
| Applicant | Stryker Leibinger GmbH & Co KG, Freiburg Im Breisgau, DE |
| Decision | Substantially Equivalent, Mar 14, 2024 |
| Received | Nov 3, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233542
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.