ClearanceBrief
510(k) K932869 ยท HRX Arthroscope

ARTHROPLANE

ApplicantSynvasive Technology, Inc., Rancho Cordova CA, US
DecisionSubstantially Equivalent, Mar 25, 1994
ReceivedJun 14, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932869

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.