ClearanceBrief
510(k) K051827 ยท HRX Arthroscope

JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE

ApplicantJoimax GmbH, Los Gatos CA, US
DecisionSubstantially Equivalent, Aug 12, 2005
ReceivedJul 6, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051827

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.