510(k) K062920 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
ORTHOFIX TITANIUM HUMERAL PLATING SYSTEM LSP
| Applicant | Orthofix Srl, Oregon City OR, US |
| Decision | Substantially Equivalent, Nov 13, 2006 |
| Received | Sep 28, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062920
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.