ClearanceBrief
510(k) K031454 ยท HAW Neurological Stereotaxic Instrument

ACUMEN SURGICAL NAVIGATION SYSTEM

ApplicantBiomet, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jul 8, 2004
ReceivedMay 7, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031454

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.