ClearanceBrief
510(k) K033508 ยท MNI Orthosis, Spinal Pedicle Fixation

PLUS PIVOT LINK UNIVERSAL SYSTEM

ApplicantSpine Vision, Inc., Atlanta GA, US
DecisionSubstantially Equivalent, Jan 27, 2004
ReceivedNov 6, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033508

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.