510(k) K991696 ยท DZI Drill, Bone, Powered
STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM
| Applicant | Stryker Instruments, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Oct 25, 1999 |
| Received | May 18, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991696
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.