ClearanceBrief
510(k) K071877 ยท MNI Orthosis, Spinal Pedicle Fixation

LANX SPINAL FIXATION SYSTEM

ApplicantLanx, LLC, Philadelphia PA, US
DecisionSubstantially Equivalent, Sep 17, 2007
ReceivedJul 9, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071877

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.