510(k) K141935 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
STRYKER S2 DRILL
| Applicant | Stryker Corporation, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Sep 26, 2014 |
| Received | Jul 17, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141935
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.