510(k) K052239 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
EBI DYNAFIX VISION FOOTPLATE SYSTEM
| Applicant | Ebi, L.P., Parsippany NJ, US |
| Decision | Substantially Equivalent, Sep 21, 2005 |
| Received | Aug 17, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052239
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.