510(k) K073633 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
STRYKER ESSX MICRODEBRIDER SYSTEM
| Applicant | Stryker Ireland Ltd., Instruments Division, Carrigtwohill, Co.Cork, IE |
| Decision | Substantially Equivalent, Aug 26, 2008 |
| Received | Dec 26, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073633
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.