ClearanceBrief
510(k) K990324 ยท HRX Arthroscope

NUVASIVE GUIDED SPINAL ARTHROSCOPY SYSTEM

ApplicantNuvasive, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Oct 5, 1999
ReceivedFeb 2, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990324

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.