ClearanceBrief
510(k) K051697 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation

SELECTIVE-AXIS POSTERIOR NONCERVICAL PLATING SYSTEM

ApplicantMedical Device Advisory Development Group, Irvine CA, US
DecisionSubstantially Equivalent, Sep 21, 2005
ReceivedJun 23, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051697

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.