ClearanceBrief
510(k) K110419 ยท GXZ Electrode, Needle

AVS ARIA NEUROMONITORING PROBE AND AVS ARIA PROBE DILATORS

ApplicantStryker Spine, Allendale NJ, US
DecisionSubstantially Equivalent, Jul 28, 2011
ReceivedFeb 14, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K110419

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.