510(k) K940710 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
STRYKER MICRODEBRIDER SYSTEM
| Applicant | Stryker Corp., San Jose CA, US |
| Decision | Substantially Equivalent, May 16, 1994 |
| Received | Feb 17, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940710
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.