ClearanceBrief
510(k) K050774 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

LANX ANTERIOR CERVICAL PLATE SYSTEM

ApplicantLanx, LLC, Pleasant Hill CA, US
DecisionSubstantially Equivalent, Apr 11, 2005
ReceivedMar 25, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K050774

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.