ClearanceBrief
510(k) K053159 ยท HAW Neurological Stereotaxic Instrument

VECTORVISION SPINE

ApplicantBrainlab AG, Heimstetten, DE
DecisionSubstantially Equivalent, Jun 6, 2006
ReceivedNov 14, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K053159

DateFirm and productCodeLinked 510(k)
Feb 10, 2014Brainlab AG
BrainLAB's VectorVision spine is intended for use as an intraoperative image-guided localization system for minimally invasive surgery. It links a freehand probe, tracked by a passive marker sensor sy
Terminated
HAWNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.