510(k) K091686 ยท HWC Screw, Fixation, Bone
LEFORTE NEUROSYSTEM BONE SCREW
| Applicant | Jeil Medical Corporation, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Nov 13, 2009 |
| Received | Jun 9, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091686
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.