ClearanceBrief
510(k) K980588 ยท GAD Retractor

CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000

ApplicantClarus Medical Systems, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 18, 1998
ReceivedFeb 17, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980588

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.