ClearanceBrief
510(k) K980184 ยท MNI Orthosis, Spinal Pedicle Fixation

CD SPINAL SYSTEM

ApplicantSofamor Danek USA,Inc., Memphis TN, US
DecisionSubstantially Equivalent, Dec 18, 1998
ReceivedJan 20, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980184

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.