ClearanceBrief
510(k) K982914 ยท MNI Orthosis, Spinal Pedicle Fixation

AESCULAP SPINE SYSTEM EVOLUTION: ADDITIONAL COMPONENTS

ApplicantAesculap, Inc., South San Francisco CA, US
DecisionSubstantially Equivalent, Oct 2, 1998
ReceivedAug 19, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982914

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.