ClearanceBrief
510(k) K981508 ยท HAW Neurological Stereotaxic Instrument

VECTORVISION SPINE MODULE

ApplicantBrainlab AG, Palo Alto CA, US
DecisionSubstantially Equivalent, Oct 29, 1998
ReceivedApr 27, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981508

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.