ClearanceBrief
510(k) K950955 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation

PARAGON POSTERIOR SPINAL SYSTEM

ApplicantSofamor Danek USA,Inc., Memphis TN, US
DecisionSubstantially Equivalent for Some Indications, Aug 25, 1995
ReceivedMar 2, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950955

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.