510(k) K171840 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
Stryker Consolidated Operating Room Equipment (CORE) 2 Console
| Applicant | Stryker Corporation, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Sep 15, 2017 |
| Received | Jun 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171840
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.