510(k) K091679 ยท JEY Plate, Bone
LEFORTE SYSTEM BONE PLATE
| Applicant | Jeil Medical Corporation, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 2, 2009 |
| Received | Jun 9, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091679
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.