ClearanceBrief
510(k) K982686 ยท MNI Orthosis, Spinal Pedicle Fixation

MODIFICATION TO TOWNLEY PEDICLE SCREW PLATING SYSTEM

ApplicantSofamor Danek USA,Inc., Memphis TN, US
DecisionSubstantially Equivalent, Aug 7, 1998
ReceivedAug 3, 1998
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K982686

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.