ClearanceBrief
510(k) K896770 ยท HRX Arthroscope

ARTHRODISTRACTOR

ApplicantArthroplastics, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jan 2, 1990
ReceivedNov 30, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896770

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.