510(k) K870217 ยท HTW Bit, Drill
FEMORAL CEMENT REMOVAL INSTRUMENTS
| Applicant | Kenneth J. Hoek, M.D., Inc., Ukiah CA, US |
| Decision | Substantially Equivalent, Feb 6, 1987 |
| Received | Jan 21, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870217
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.