ClearanceBrief
510(k) K050897 ยท HAW Neurological Stereotaxic Instrument

NAVIPRO SHOULDER SOFTWARE MODULE

ApplicantKinamed, Inc., Camarillo CA, US
DecisionSubstantially Equivalent, May 24, 2005
ReceivedApr 8, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K050897

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.