510(k) K882407 ยท LXI Guide, Drill, Ligament
BOW & ARROW DRILL GUIDE
| Applicant | Instrument Makar, Inc., Okemos MI, US |
| Decision | Substantially Equivalent, Sep 6, 1988 |
| Received | Jun 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882407
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.