ClearanceBrief
510(k) K021748 ยท HRX Arthroscope

ENDIUS ATAVI SYSTEM

ApplicantEndius, Inc., Plainville MA, US
DecisionSubstantially Equivalent, Jun 26, 2002
ReceivedMay 28, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K021748

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.