ClearanceBrief
510(k) K103192 ยท HAW Neurological Stereotaxic Instrument

NAVIGATION MARKER, REFLECTIVE MARKER SPHERES

ApplicantIlumark GmbH, Muhlheim, DE
DecisionSubstantially Equivalent, Feb 7, 2011
ReceivedOct 29, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103192

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.