ClearanceBrief
510(k) K010612 ยท HAW Neurological Stereotaxic Instrument

VECTORVISION KNEE

ApplicantBrainlab AG, Heimstetten, DE
DecisionSubstantially Equivalent, Sep 6, 2001
ReceivedMar 1, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010612

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.