510(k) K122541 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
ORTHOFIX CONTOURS PROIMAL HUMERAL PLATE (PHP)
| Applicant | Orthofix Srl, West Linn OR, US |
| Decision | Substantially Equivalent, Sep 20, 2012 |
| Received | Aug 21, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122541
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.