510(k) K071612 ยท JEY Plate, Bone
MODUS TRILOCK 2.0/2.3/2.5
| Applicant | Medartis AG, San Diego CA, US |
| Decision | Substantially Equivalent, Sep 11, 2007 |
| Received | Jun 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071612
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.