ClearanceBrief
510(k) K132403 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation

ANNEXTM ADJACENT LEVEL SYSTEM

ApplicantSpine Wave, Inc., Shelton CT, US
DecisionSubstantially Equivalent, Jan 10, 2014
ReceivedAug 1, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132403

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.