510(k) K892903 ยท HTW Bit, Drill
MITEK ANCHOR DRILL
| Applicant | Mitek Surgical Products, Inc., Dedham MA, US |
| Decision | Substantially Equivalent, Oct 6, 1989 |
| Received | Apr 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892903
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.