510(k) K162341 ยท OLO Orthopedic Stereotaxic Instrument
Stryker OrthoMap Precision Knee system
| Applicant | Stryker Leibinger GmbH & Co KG, Freiburg, DE |
| Decision | Substantially Equivalent, Oct 12, 2016 |
| Received | Aug 22, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162341
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.