510(k) K172034 ยท OLO Orthopedic Stereotaxic Instrument
Stryker Spine Navigation System with SpineMap 3D software application, OrthoLock, nGenius Spine Clamp, Navigated Drill Guide Set, Navigated Xia 3 Awl Tap, Navigated Xia 3 Serrato Tap
| Applicant | Stryker Corporation, Freiburg, DE |
| Decision | Substantially Equivalent, Oct 18, 2017 |
| Received | Jul 5, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172034
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.