ClearanceBrief
510(k) K954789 ยท HAW Neurological Stereotaxic Instrument

BRAINLAB HEADPINS

ApplicantBrainlab AG, Moorestown NJ, US
DecisionSubstantially Equivalent, Aug 12, 1996
ReceivedOct 18, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954789

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.