ClearanceBrief
510(k) K081165 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation

ELLIPSE LUMBAR POSTERIOR OSTEOSYNTHESIS SYSTEM

ApplicantSpineart, Geneva, CH
DecisionSubstantially Equivalent, Dec 17, 2008
ReceivedApr 24, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081165

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.