ClearanceBrief
510(k) K032398 ยท MNI Orthosis, Spinal Pedicle Fixation

PLUS PIVOT LINK UNIVERSAL SYSTEM

ApplicantSpine Vision, Inc., Atlanta GA, US
DecisionSubstantially Equivalent, Oct 31, 2003
ReceivedAug 4, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032398

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.