510(k) K070393 ยท HWC Screw, Fixation, Bone
LAGWIRE SYSTEM
| Applicant | Fxdevices, Boca Raton FL, US |
| Decision | Substantially Equivalent, May 4, 2007 |
| Received | Feb 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070393
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.