ClearanceBrief
510(k) K060967 ยท NDQ System, Catheter Or Guidewire, Steerable (Magnetic)

NIOBE MAGNETIC NAVIGATION SYSTEM W/NAVIGANT WORKSTATION

ApplicantStereotaxis, Inc., St. Louis MO, US
DecisionSubstantially Equivalent, Oct 19, 2006
ReceivedApr 7, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060967

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.