ClearanceBrief
510(k) K950596 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation

GDLH POSTERIOR SPINAL SYSTEM

ApplicantSofamor Danek USA,Inc., Memphis TN, US
DecisionSubstantially Equivalent for Some Indications, Aug 28, 1995
ReceivedFeb 9, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950596

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.