510(k) K080052 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
STRYKER ESSX WITH NAVIGATION MOUNT
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Oct 2, 2008 |
| Received | Jan 8, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080052
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.