ClearanceBrief
510(k) K882053 ยท GYC Electrode, Cortical

NICOLET EPIDURAL SPINAL ELECTRODE

ApplicantNicolet Instrument Corp., Madison WI, US
DecisionSubstantially Equivalent, Oct 18, 1988
ReceivedMay 16, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882053

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.