ClearanceBrief
510(k) K160811 ยท HAW Neurological Stereotaxic Instrument

CRW STEREOTACTIC SYSTEM

ApplicantIntegra LifeSciences Corporation, Planisboro NJ, US
DecisionSubstantially Equivalent, Dec 6, 2016
ReceivedMar 24, 2016
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K160811

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.