ClearanceBrief
510(k) K131833 ยท KWP Appliance, Fixation, Spinal Interlaminal

CENTURION POCT SYSTEM

ApplicantOrthofix, Inc., Lewisville TX, US
DecisionSubstantially Equivalent, Jan 30, 2014
ReceivedJun 20, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K131833

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.