ClearanceBrief
510(k) K071435 ยท MNI Orthosis, Spinal Pedicle Fixation

NUVASIVE OCT SYSTEM

ApplicantNuvasive, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Aug 6, 2007
ReceivedMay 23, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071435

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.