510(k) K992106 ยท HWC Screw, Fixation, Bone
MODUS SYSTEM SELF-DRILLING SCREWS
| Applicant | Medartis AG, Waltham MA, US |
| Decision | Substantially Equivalent, Sep 17, 1999 |
| Received | Jun 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992106
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.